Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Tonsillitis from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 12
- Active, not recruiting: 4
- Completed: 23
- Other: 11
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT04083417 — Sore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and No Antibiotic Treatment
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Katarina Hedin |
| Enrollment | 260 |
| Study Type | INTERVENTIONAL |
| Conditions | Sore Throat; Tonsillitis |
| Interventions | ; |
Sore throat is the second most common cause of antibiotic prescribing in primary care in Sweden. Guidelines for sore throat focus on identifying people with sore throat where there are 3 and 4 specified criteria and where near patient tests identify group A streptococci (GAS). In these cases, phenoxymethylpenicillin is recommended.
Studies that have identified microorganisms in sore throat sho…
NCT05575401 — Lateral Pharyngoplasty Outcomes in Children Undergoing Tonsillectomy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Loma Linda University |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep-Disordered Breathing; Sleep Apnea Syndromes in Children; Sleep Apnea, Obstructive; Tonsillitis; Tonsillar Hypertrophy |
| Interventions | ; |
The goal of this treatment study is to determine if doing lateral pharyngoplasty with tonsillectomy is better for children than doing tonsillectomy alone. The main questions it aims to answer are:
- Do children experience less pain after surgery when lateral pharyngoplasty is performed with tonsillectomy compared to tonsillectomy alone?
- Do children eat/drink better when lateral pharyngoplast…
NCT05656365 — Evaluating the Genetics and Immunology of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) Syndrome and Other Tonsil Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Periodic Fever, Aphthous Stomatitis, Pharyngitis, And Cervical Adenitis (Pfapa); Obstructive Sleep Apnea; Tonsillitis; Tonsil Disorder; Sleep Disordered Breathing |
Background:
Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) is the most common periodic fever syndrome of childhood. Symptoms can include swelling of the glands in the throat, mouth ulcers, and tonsillitis. Removal of the tonsils can stop the periodic flareups. But researchers do not know how PFAPA develops. In this natural history study, researchers will collec…
NCT06023550 — Complicated Infections in Otorhinolaryngology
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Medical Centre Ljubljana |
| Enrollment | 2550 |
| Study Type | OBSERVATIONAL |
| Conditions | Sinusitis; Otitis; Laryngitis; Lymphadenitis; Quinsy |
| Interventions |
This observational study aims to learn more about complicated infections treated by otorhinolaryngologists. The main questions to answer are:
- What is the management of complicated sinonasal infections in Ljubljana, Slovenia,
- What is the management of complicated ear and temporal bone infections in Ljubljana, Slovenia,
- What is the management of complicated neck soft tissue infections in L…
NCT06606262 — Tonsillectomy Versus Tonsillotomy in the Treatment of Recurrent Acute Tonsillitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Tejs Ehlers Klug |
| Enrollment | 250 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis Recurrent |
| Interventions | ; |
Background: recurrent acute tonsillitis (RT) is a frequent condition affecting teenagers and adults. Patients suffer from recurring throat symptoms, fever and impaired quality of life (QOL). Tonsillectomy (TE) is the only well-known treatment, but studies indicate that tonsillotomy (TO) is associated with less morbidity (eg. pain and bleeding) and equal efficiency (e.g. reduced number of sore t…
NCT06576830 — Optimization of Pediatric Tonsillectomy to IMprove AnaLgesia
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Duke University |
| Enrollment | 440 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain, Postoperative; Tonsillar Hypertrophy; Tonsillitis; Pediatric Sleep Apnea; Sleep-Disordered Breathing |
| Interventions | ; |
The purpose of this study is to compare the use of short acting opioids (fentanyl/hydromorphone) with long acting opioids (methadone) for pain control following tonsillectomy surgery in children and adolescents.
NCT07035314 — The Effect of Systemic Nonsteroidal Anti-inflammatory Drugs (NSAIDs) Vs Intraoperative Infiltration of Steroids in Tonsillar Bed Following Tonsillectomy on Post Tonsillectomy Pain.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis Chronic; Tonsillitis Recurrent; OSA - Obstructive Sleep Apnea |
| Interventions | ; ; |
The aim of this study is to compare the efficacy of adding paracetamol to systemic non-steroidal anti-inflammatory drugs (NSAIDs) versus adding dexamethasone as local infiltration to paracetamol on post tonsillectomy pain control.
NCT06543823 — ST250 as a Therapeutic Option for Head & Neck Reconstruction
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Alaa Emara |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; |
To assess the use of SupraThel 250 for mucosal reconstruction in the Head & Neck region. The membrane will be applied after tonsillectomy procedures and compared to bare wounds’ healing
NCT06982105 — Trimethoprim-sulfamethoxazole vs. Clindamycin for the Treatment of Children With Invasive MRSA Infections
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Indiana University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Methicillin Resistant Staphylococcus Aureus; Osteomyelitis Acute; Septic Arthritis; Orbital Cellulitis; Facial Cellulitis |
| Interventions |
The goal of this clinical trial is to learn if trimethoprim-sulfamethoxazole (TMP-SMX) works to treat invasive infections due to methicillin-resistant Staphylococcus aureus (MRSA) in children. It will also learn about the safety of TMP-SMX in the treatment of children with invasive MRSA infections. The main questions it aims to answer are:
-Is TMP-SMX effective at successfully treating childre…
NCT07577232 — Transoral Ultrasound Versus no Transoral Ultrasound in Diagnostic Workup of Peritonsillar Abscess
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Rigshospitalet, Denmark |
| Enrollment | 368 |
| Study Type | INTERVENTIONAL |
| Conditions | Peritonsillar Abscess; Peritonsillar Cellulitis; Tonsillitis |
| Interventions |
Peritonsillar abscess (PTA) is a collection of pus between the palatine tonsil and the constrictor muscle. PTA is detected by recognizing characteristics during clinical examination: redness, pain, malaise, trismus, and unilateral peritonsillar swelling. Clinical assessment, including inspection and palpation, is the traditional diagnostic method for patients suspected of having PTA. If PTA is …
NCT07235826 — Evaluation of the Efficacy of Streptococcus Salivarius Evol12® in the Reduction of Recurrent Adenotonsillitis in Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Liaquat University of Medical & Health Sciences |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Tonsillitis |
| Interventions | ; |
This prospective, multicenter, randomized, double-blind, placebo-controlled, cross-over clinical trial will evaluate the efficacy and safety of Streptococcus salivarius Evol12® (Bactoblis® Evol) in reducing the recurrence and duration of acute febrile adenotonsillitis in children aged 3 to 11 years. Participants will receive either the probiotic or a matching placebo for 3 months, followed by a…
NCT07093749 — Perspectives on Antibiotics and Tracking Symptoms in Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Murdoch Childrens Research Institute |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Urinary Tract Infection; Cellulitis; Impetigo; Pharyngitis; Tonsillitis |
| Interventions |
The study will assess families’ perspectives and decision-making regarding the duration of oral antibiotic courses prescribed to children (4-17 years) who present with uncomplicated bacterial infections at the Royal Children’s Hospital (RCH) Emergency Department (ED). The study will involve (i) children discharged from ED on oral antibiotics and (ii) children transferred to Hospital-in-the-Home…
Active, Not Recruiting
NCT01866540 — Immune Response To Intranasal Influenza Vaccination
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Bergen |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis, Hypertrophy |
| Interventions |
This research during the last decade has focused on the kinetics of the systemic and local immune response to parenteral influenza vaccine in humans. The investigators have shown that normally high numbers of influenza specific antibody secreting cells (ASC) are present in the nasal mucosa of healthy adults but upon parenteral vaccination the numbers remain stable. However, a rapid transient in…
NCT03654742 — Intracapsular Tonsillectomy in Adults
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Turku University Hospital |
| Enrollment | 167 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsil Disease; Tonsillitis; Tonsillitis Acute; Tonsillitis Chronic |
| Interventions |
Comparing the classical extracapsular tonsillectomy (TE) performed with electrosurgery to intracapsular approaches (SIPT) by coblation or microdebrider. The patient group is adults with recurrent or chronic tonsillitis
NCT04682964 — Bacteriophage Therapy in Tonsillitis
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Tashkent State Medical University (Tashkent Pediatric Medical Institute), Uzbekistan |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Tonsillitis |
| Interventions |
The patients received bacteriophage therapy with a liquid piobacteriophage complex (liquid pyobacteriophage complex - PCL). PСL was administered via nebulizer inhalation to irrigate the tonsil mucosa. A total of 5 ml of PCL was inhaled for 10 minutes every 5 days. The drug causes the lysis of certain bacteria, including staphylococcus, enterococcus, streptococcus, enteropathogenic E. coli, Prot…
NCT07265531 — A Comparative Study of Monopolar Versus Bipolar Electrocautery Post Tonsillectomy Outcomes.
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Indus Hospital and Health Network |
| Enrollment | 74 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Tonsillitis |
This study aims to compare surgical techniques (monopolar and bipolar electrocautery -used during tonsillectomy,a common procedure to remove toonsils.The goal is to determine which method results in less pain and bleeding for patients after surgery .
Not Yet Recruiting
NCT07176533 — Suprazygomatic Maxillary Nerve Block in Pediatric Tonsillectomy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph’s |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; |
Tonsillectomies are among the most common surgical procedures performed in pediatric populations, with more than 14,000 procedures performed annually in Ontario, with more than 80% being performed to treat sleep-disordered breathing, including sleep apnea. Despite being a routine procedure, postoperative pain is a prevalent challenge following tonsillectomies, with significant pain lasting 7 to…
NCT07569939 — Evaluation of Treatments for Sore Throat Associated With Acute Pharyngitis and/or Viral Tonsillitis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Pharyngitis; Viral Sore Throat |
| Interventions | ; ; |
The objective of this study is to conduct post-marketing clinical follow-up of four products: HMG, PHN, PHR, and TUR. This follow-up will consist of collecting clinical data in real-life conditions to confirm the tolerance, safety, and efficacy of medical devices used in the treatment of sore throats related to acute pharyngitis and/or viral-origin tonsillitis, while also assessing the benefit/…
NCT07598201 — Recovery From Tonsil Surgery.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Turku University Hospital |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Tonsillitis; Chronic Tonsillitis |
| Interventions | ; |
The goal of this study is to optimize the duration of sick leave and the usage of opioids following partial tonsillar surgery in adults by comparing the recovery after extracapsular tonsillectomy (ECTE) with recovery after intracapsular tonsillectomy (ICTE). An additional objective is to confirm that ICTE is as effective as ECTE when comparing TOI-14 scores after 12 months post-operatively.
Th…
Completed Trials
NCT01361399 — Active and Placebo Controlled Study to Test the Efficacy and Safety of an Aspirin-Lidocaine Lozenge in the Symptomatic Treatment of Sore Throat Associated With a Common Cold
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Bayer |
| Enrollment | 1088 |
| Study Type | INTERVENTIONAL |
| Conditions | Common Cold; Pharyngitis; Tonsillitis |
| Interventions | ; ; |
The purpose of this study is to investigate the analgesic efficacy of a single dose of a fixed combination of 500 mg Aspirin (Acetylsalicylic Acid) and 4 mg Lidocaine in adult patients with sore throat associated with a common cold in comparison to a single treatment with 500 mg Aspirin or 4 mg Lidocaine alone as well a Placebo (treatment without any active ingredient). The combination of Aspir…
NCT00654511 — Dexmedetomidine for Immediate Perioperative Analgesia in Pediatric Patients Undergoing Tonsillectomy
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Children’s National Research Institute |
| Enrollment | 101 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; ; |
The primary purpose of this study is:
- To compare dexmedetomidine with fentanyl in terms of intra-operative hemodynamics and post-operative analgesia.
- To determine an analgesic dose response relationship for dexmedetomidine.
- Compare recovery characteristics of dexmedetomidine to fentanyl.
NCT00829972 — Vitamin D Levels in Children Undergoing Adenotonsillectomies and Controls
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Tonsillitis |
The investigators aim to evaluate the levels of serum Vitamin D in children having their tonsils removed and appropriate controls. The investigators hypothesize that children undergoing tonsil removal will have lower Vit D levels than accepted norms and when compared to controls. The investigators also hypothesize that Vitamin D deficiency will correlate with indicators of inflammation such as …
NCT01255670 — Penicillin and Metronidazole in Treatment of Peritonsillar Abscess
| Status | Completed |
| Phase | N/A |
| Sponsor | Helsinki University Central Hospital |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Peritonsillar Abscess |
| Interventions |
Treatment of peritonsillar abscess varies. To study whether broad spectrum antibiotics are required in addition to abscess drainage, a prospective, double blind, placebo-controlled, randomized study on 200 adult patients with peritonsillar abscess is performed. 100 patients are given penicillin and metronidazole and 100 patients get penicillin and placebo. Recovery and recurrence are analyzed.
NCT01695980 — Laryngeal Mask Airway in Pediatric Adenotonsillectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Eastern Virginia Medical School |
| Enrollment | 81 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep Apnea, Obstructive; Tonsillitis |
| Interventions | ; |
The study will compare how often the tubing kinks when a LMA (laryngeal mask airway) with modified retractor is used compared to use of an endotracheal tube (ETT) and non modified retractor is used.
NCT02858687 — Improving the Diagnosis of Tonsillitis in Emergency Rooms
| Status | Completed |
| Phase | N/A |
| Sponsor | Assistance Publique Hopitaux De Marseille |
| Enrollment | 312 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions |
A point-of-care laboratory (POC) was set at North Hospital, Marseille, France for the diagnosis in less than two hours of tonsillitis caused by known pathogens, close to the reception of Emergency service. In this instance 30% of patients have no etiological diagnosis after the POC tonsillitis tests . This lab has discovered over 200 new species of bacteria in humans, including vector bacteria …
NCT03408704 — Antimicrobial Stewardship Program (ASP) in Patients With a Sore Throat
| Status | Completed |
| Phase | N/A |
| Sponsor | Vastra Gotaland Region |
| Enrollment | 49 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis; Streptococcus Pharyngitis; Sore Throat; Pharyngitis; Pharyngitis Bacterial |
| Interventions |
The investigators have developed an antibiotic stewardship program (ASP) to increase adherence to the Swedish guidelines for managing patients with a sore throat. This is a randomized controlled trial where primary health care centers are randomised to get the ASP or not. The adherence to the Swedish guidelines are measured in all participating centers.
NCT03995628 — Steroids and Pain Control After Tonsillectomy
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Medical University of South Carolina |
| Enrollment | 163 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis; Obstructive Sleep Apnea of Child |
| Interventions | ; |
This research study aims to find out if a single oral dose of steroid after tonsillectomy will reduce pain and decrease the need for narcotic medications.
NCT03793816 — Tonsillectomy Using BiZact™ - a Randomized Side-controlled Clinical Trial
| Status | Completed |
| Phase | N/A |
| Sponsor | Medical University of Vienna |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis Chronic; Tonsillectomy; Hemorrhage; Postoperative Pain; Postoperative Hemorrhage |
| Interventions |
Tonsillectomies are frequently followed by severe postoperative pain, hence high analgetics consumption and prolonged hospitalization. Also, postoperative hemorrhages can be hazardous. Constant evaluation of surgical techniques is paramount to improve safety and cost-effectiveness. Frequently tonsillectomies are performed in cold steel technique. Aim of this study will be the evaluation of hand…
NCT04230681 — Hydromorphone vs Fentanyl in Children Undergoing Tonsillectomy Surgery
| Status | Completed |
| Phase | Early Phase 1 |
| Sponsor | Washington University School of Medicine |
| Enrollment | 189 |
| Study Type | INTERVENTIONAL |
| Conditions | Obstructive Sleep Apnea; Tonsillitis |
| Interventions | ; |
A RCT to compare hydromorphone versus fentanyl for pain control following tonsillectomy or adenotonsillectomy surgery.
NCT04277299 — Intelligent Customer-driven Solution for Children and Their Parents Undergoing Day Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Oulu |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis; Herniorrhaphies; Surgery; Children; Parents |
| Interventions |
This research aims to evaluate the effectiveness of web-based mobile intervention (Icory -Solution) developed to pediatric patients and their parents in the pathway of outpatient surgery treatment in pre-intra- and postoperative setting: (1) Examine the effectiveness of the intervention on children’s preoperative anxiety and fear, and postoperative pain (2) examine the effectiveness of the inte…
NCT05532228 — Evaluation of the Functional Impact of Adenotonsilectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Instituto de Ciências Biomédicas Abel Salazar |
| Enrollment | 78 |
| Study Type | OBSERVATIONAL |
| Conditions | Apnea, Obstructive; Tonsillitis; Tonsillar Hypertrophy; Respiratory Function Impaired; Infections |
| Interventions |
Spirometric assessment of respiratory function before and after adenotonsillectomy surgery
NCT04551196 — Management of Post-Tonsillectomy Pain in Pediatric Patients
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Washington University School of Medicine |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain, Postoperative; Tonsillar Hypertrophy; Tonsillitis |
| Interventions | ; |
Single-center, randomized, open-label, non-inferiority treatment pilot study to evaluate the effectiveness of a combined acetaminophen and ibuprofen regimen for treatment of post-operative tonsillectomy pain in the pediatric population. 100 children undergoing tonsillectomy will be randomized to receive either a combined acetaminophen and ibuprofen regimen dosed every 6 hours or an alternating …
NCT04657549 — Tonsil Surgery in Recurrent or Chronic Tonsillitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Oulu University Hospital |
| Enrollment | 147 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis Recurrent; Tonsillitis Chronic |
| Interventions | ; |
Tonsil surgery is common in adults with recurrent or chronic tonsillitis. The surgical techniques include either partial or total surgical removal of the palatal tonsils (tonsillotomy, TT, and tonsillectomy, TE, respectively). The aim of this study is to find out, whether tonsil surgery improves the quality of life in these patients and whether the lighter TT is as effective as TE. Our main out…
NCT04725305 — BiZact Tonsillectomy in the Pediatric Population
| Status | Completed |
| Phase | N/A |
| Sponsor | Baylor College of Medicine |
| Enrollment | 144 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillectomy; Tonsillitis Chronic; Hemorrhage; Postoperative Pain; Postoperative Hemorrhage |
| Interventions | ; |
This study has been designed to evaluate how effective the Bizact tonsillectomy device is in reducing operating time and complications that occur after surgery. This device operates in a different way than the standard device that is used for most tonsillectomies. In 2019, a study was conducted in 186 children and adults using this device in tonsillectomies. Results showed lower blood loss and …
NCT05244226 — Pediatric Pain Optimization After Tonsillectomy
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Duke University |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Obstructive Sleep Apnea; Tonsillitis; Pain, Procedural |
| Interventions | ; |
The purpose of this study is to compare the use of short acting opioids (fentanyl/hydromorphone) with long acting opioids (methadone) for pain control following tonsillectomy surgery.
NCT06494839 — Outcomes of Bipolar Electrocautery Tonsillectomy Versus Cold Steel Dissection Pediatric Tonsillectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | RESnTEC, Institute of Research |
| Enrollment | 110 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; |
It was intended to practically establish whether or not the relatively newer technique of tonsillectomy like bipolar electrocautery tonsillectomy has any added benefits in reducing the duration of surgery, blood loss and post-operative pain as compared with conventional cold steel dissection method. This study was done to compare the outcomes of bipolar electrocautery tonsillectomy versus cold …
NCT06184477 — The Relationship Between Prolonged Hospitalization and Surgical Experience in Pediatric Tonsillectomy Cases.
| Status | Completed |
| Phase | N/A |
| Sponsor | Pamukkale University |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Sleep Apnea; Tonsillitis Recurrent |
| Interventions |
Guided by the expertise of a seasoned surgeon at the tertiary care hospital, the training program includes performing tonsillectomy starting from the 6th month. The clinical protocol at the hospital dictates a standard one-night hospital stay for all patients, but there is potential to extend the duration in specific cases. The study endeavors to explore the correlation between extended hospita…
NCT07675278 — Comparing Two Agents Used to Stop Bleeding During Tonsil Removal Surgery: Adrenaline Versus Hydrogen Peroxide
| Status | Completed |
| Phase | N/A |
| Sponsor | Rawalpindi Medical College |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Tonsillitis; Tonsillar Hypertrophy, Tonsillitis; Tonsillectomy |
| Interventions | ; |
The goal of this quasi-experimental study is to compare the effectiveness of topical adrenaline and 3% hydrogen peroxide for controlling bleeding (hemostasis) during tonsil removal surgery in patients aged 5 to 18 years. The main questions it aims to answer are: 1. Which substance leads to faster bleeding control during surgery? 2. Which substance results in less total blood loss during surgery…
NCT06326983 — Opioid Sparing Anesthesia Care for Pediatric Patients Having Tonsil Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | Boston Children’s Hospital |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis; Post-operative Nausea and Vomiting (PONV); Emergence Delirium; Opioid Analgesic Adverse Reaction; Anesthesia |
| Interventions | ; ; |
This is a prospective, randomized, controlled, non-inferiority study of patients undergoing tonsil surgeries at Boston Children’s Hospital Waltham. The overall aim is to evaluate the efficacy of an opioid anesthetic plan (morphine, ketorolac, and acetaminophen versus an opioid sparing anesthetic plan (dexmedetomidine, ketorolac and acetaminophen) for perioperative analgesia and recovery time in…
NCT06937762 — Coblation Tonsillotomy Versus Radiofrequency and Cold Knife Dissection Tonsillectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Kafrelsheikh University |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Tonsillitis |
| Interventions | ; ; |
This study aims to assess and compare the outcomes between coblation intracapsular tonsillotomy versus extracapsular Radiofrequency and cold knife dissection tonsillectomy efficacy in managing patients requiring tonsil surgery as regards (time of operation, Intraoperative blood loss, postoperative pain, postoperative bleeding, complications, tonsillar fossa healing)
NCT07656831 — Study Comparing Harmonic Scalpel and Conventional Cold Steel Tonsil Removal Surgery in Children Requiring Tonsillectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Allama Iqbal Teaching Hospital |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Tonsillitis |
| Interventions | ; |
This clinical trial aims to compare two commonly used methods of tonsil removal surgery (tonsillectomy) in children and adults with chronic tonsillitis. Chronic tonsillitis refers to repeated episodes of tonsil infection that occur frequently over several years and require surgical removal of the tonsils.
The main question this study aims to answer is:
Does tonsillectomy performed with a harm…
NCT07457619 — Coblation Tonsillectomy Versus Cold Dissection Tonsillectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Shahida Islam Medical Complex |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; |
The surgical removal of the tonsils is known as a tonsillectomy. Even though tonsillectomy rates have decreased recently, it is still one of the most common surgical operations carried out globally.1 In 30 BC, Celsus was the first to describe tonsil removal. Since then, a variety of surgical techniques and better tools have been developed for this aim.2 Postoperative discomfort and hemorrhage a…
Other (Suspended)
NCT02471599 — Effect of Tonsillectomy on Longterm Renal Outcome of IgA Nephropathy
| Status | Suspended |
| Phase | N/A |
| Sponsor | Sun Yat-sen University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | IgA Nephropathy |
| Interventions | ; |
The effect of tonsillectomy therapy on IgA nephropathy is still controversial.Few prospective,randomized investigations have examined how tonsillectomy affects the shortterm and longterm renal outcome of IgA nephropathy.This is A prospective,randomized ,controlled study to explore the longterm effect of tonsillectomy for patients with IgA nephropathy.
Other (Unknown)
NCT03323047 — Perioperative Tonsillectomy Protocol Development
| Status | Unknown |
| Phase | Phase 4 |
| Sponsor | London Health Sciences Centre |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; ; |
Pediatric patients who are undergoing a tonsillectomy at the Children’s hospital will be randomly assigned to one of three drug groups: 1) acetaminophen (Tylenol) administered pre-operatively and a low dose of anti-inflammatory drug (dexamethasone) administered intra-operatively; 2) acetaminophen (Tylenol) administered pre-operatively and a high dose of anti-inflammatory drug (dexamethasone) ad…
NCT03292068 — Children Recovering From Tonsil Surgery
| Status | Unknown |
| Phase | N/A |
| Sponsor | Lund University |
| Enrollment | 576 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillitis |
| Interventions | ; ; |
Children recovering from tonsil surgery following day surgery Tonsil surgery - self-care and treatment - the TONIST-study The main objective of this study is to evaluate the effect and experience of acupuncture, acupressure, specially designed diet and telephone counselling on children’s surgery-related symptoms, quality of life and costs during recovery after tonsillectomy (TE) or tonsillotomy…
Other (Terminated)
NCT04528173 — Opioid-Free Anesthetic for Tonsillectomy
| Status | Terminated |
| Phase | Phase 4 |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Anesthesia; Opioid Use; Tonsillitis; Sleep Disorder; Surgery |
| Interventions | ; ; |
Prospective randomized controlled trial to determine if opioid-free anesthetic for tonsillectomy is non-inferior to standard opioid-containing anesthetic
Other (Withdrawn)
NCT04998513 — Medical Versus Surgical Treatment for Peritonsillar Abscesses
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | Nova Scotia Health Authority |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Peritonsillar Abscess; Surgical Incision |
| Interventions | ; |
Peritonsillar abscesses are major infections around the tonsils. The abscess is a collection of pus that can cause a large amount of pain and discomfort, which can result in trouble swallowing and drinking. Peritonsillar abscesses must be treated because they can spread to other areas in the throat and neck, which can cause difficulty breathing, can even spread throughout the rest of the body. …
NCT05279534 — Efficacy and Safety of L. Plantarum and P. Acidilactici in Children With Upper Respiratory Tract Infections
| Status | Terminated |
| Phase | N/A |
| Sponsor | AB Biotics, SA |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Upper Respiratory Tract Infections; Pharyngitis; Tonsillitis |
| Interventions | ; |
Randomized, placebo-controlled trial to evaluate the coadjuvant effect of a combination of L. plantarum and P. acidilactici probiotic strains, taken twice daily, in children 6 months to 5 years-old with upper respiratory tract infections with pharyngitis and/or tonsillitis. Main objective is to evaluate efficacy of this probiotic in reducing fever and pain, as well to evaluate its safety.
NCT06391151 — Effect of OSA Resulting From Chronic Tonsillitis on Pregnancy Outcomes
| Status | Unknown |
| Phase | N/A |
| Sponsor | Peking University First Hospital |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Obstructive Sleep Apnea; Chronic Tonsillitis; Pregnancy |
| Interventions |
This cohort study aims to investigate the impact of obstructive sleep apnea hypopnea syndrome (OSA) resulting from chronic tonsillitis on pregnancy outcomes. The hypothesis posits that chronic tonsillitis-induced OSA may exacerbate pregnancy complications and increase the risk of adverse pregnancy outcomes.
NCT06478433 — Study on the Efficacy and Safety of a Device for Post-op Recovery in Pediatric Adenectomy/Adenotonsillectomy.
| Status | Unknown |
| Phase | N/A |
| Sponsor | Pharmaluce srl |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Adenoidal Disorder; Tonsillitis; Otorhinolaryngologic Diseases; Nasal Disease |
| Interventions | ; |
The objective of this prospective pre-market interventional clinical study is to evaluate the efficacy and safety of the medical device Munatoril® Aerosol Combo in its different modalities of use, through the analysis of clinical and subjective outcomes in children operated on adenoidectomy or adenotonsillectomy, compared with a hypertonic solution and an over-the-counter isotonic solution (con…