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A study to compare different injections to reduce swelling and pain during wisdom tooth removal

Efficacy of submucosal Injection Aprotonin, Hyaluronidase and Dexamethasone during third molar surgery : A randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091794
Enrollment
51
Registered
2025-07-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Aprotinin: Injection Aprotinin 2ml administered submucosally just before the incision single dose.Total duration is single administration on the day of surgery only Intervention2: Hyalu

Sponsors

All India Institute of Medical Sciences Rajkot
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy ambulatory patients reporting to the Department of Dentistry, AIIMS Rajkot requiring removal of single impacted lower third molars which necessitates mucoperiosteal flap elevation, buccal bone guttering with or without sectioning of tooth, Age between 18-50 years, slight and moderate difficult impaction based on radiographs.

Exclusion criteria

Exclusion criteria: Patients with systemic diseases, pregnancy and breast-feeding or any other medicinal therapy that could interfere with healing process, use of any antibiotic or any anti-inflammatory drug within 1 week period, patient with preoperative swelling, reduced mouth opening, any abusive habits like tobacco chewing, alcohol consumption and smoking.

Design outcomes

Primary

MeasureTime frame
Postoperative facial swelling measured in millimeters using linear facial measurements.Timepoint: Baseline(preoperatively),72 hrs, 7 days

Secondary

MeasureTime frame
Change in interincisal mouth opening (in mm)Timepoint: Baseline(preoperatively),72 hrs, 7 days;Reduction in pain measured using Visual Analog Scale (VAS)Timepoint: Baseline(preoperatively),72 hrs, 7 days

Countries

India

Contacts

Public ContactDr Shreeya Sharma

All India Institute of Medical Sciences, Rajkot, Gujarat

shreeyasharma231@gmail.com8830388570

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026