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Comparing the usefulness of two drugs in providing relief for swelling and pain after surgical removal of lower third molar teeth.

Phase 4
Completed
Conditions
Health Condition 1: Z488- Encounter for other specified postprocedural aftercare
Registration Number
CTRI/2020/07/026443
Lead Sponsor
Department of OMFS OHSC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

Patients with bilateral impacted mandibular third molars diagnosed for surgical extraction.

Exclusion Criteria

1.Pregnant and lactating women

2.Patients on anticoagulant therapy

3.Patients allergic to bromelain or Diclofenac Sodium

4.Use of any antibiotic or anti-inflammatory drug within 2 weeks of study entry

5.Patients with history of peptic ulcer disease/GI bleed

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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