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A study to see the analgesic and safety efficacy of Tab. Diclofenac sodium and Tab. Etodolac

Phase 4
Conditions
Health Condition 1: null- Patient with surgical removal of third molar tooth
Registration Number
CTRI/2016/11/007437
Lead Sponsor
Sir Takhtsinhaji General Hospital and Government Medical College Bhavnagar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

1.Duration of acute pain less than 4 hours

Participant willing to give written informed consent

2.Participants with impacted mandibular third molar tooth

Exclusion Criteria

1.Participants with a history of sensitivity to any drugs.

2.Participants with injury to teeth.

3.Participants with acute pain more than 4 hours.

4.Participant with history of Valvular Heart Disease; Bypass surgery within 6 months; on anticoagulant drugs.

5.Pregnant or lactating women.

6.Participants who were unable to continue for the proposed length of treatment or return for follow-up visits.

7.Participant not willing to give written informed consent.

8.Participants with an uncontrolled Diabetes, Hypertension, Neoplasm.

9.Participant with known neuropsychiatric illness.

10.Participants with blood dyscrasia or coagulation disorders.

11.Participants having consumption of drugs of abuse or taken pain medication in the previous 24 hours.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Compare safety and analgesic efficacy of Diclofenac sodium with Etodolac after surgical removal of third molar tooth in terms of Visual Analogue Scale.Timepoint: 0,2,6,24,48,72 hours
Secondary Outcome Measures
NameTimeMethod
The mean time to onset of analgesia, Time to maximum pain relief, Total pain relief and Summed Pain Intensity Difference. <br/ ><br>ï?? The degree of pain relief, Global evaluation (PGE: excellent, very good, good, fair, or poor) <br/ ><br>Timepoint: 0,2,6,24,48,72 hours
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