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Rectal Versus Oral Diclofenac Sodium in Relieving Post Episiotomy Pain

NCT04331210 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1024

Last updated 2020-04-02

No results posted yet for this study

Summary

Current study aims to compare oral diclofenac sodium with it's rectal form for analgesia of pain after episiotomy.

Conditions

  • Episiotomy Wound

Interventions

DRUG

Diclofenac Sodium

Group 1 will take oral diclofenac sodium and group 2 will take Rectal diclofenac sodium as an analgesic

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Principal Investigators

  • Diaa eldin Mohammed, Professor · women health hospital assiut university

  • Osama Saber, Lecturer · women health hospital assiut university

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-09-01
Primary Completion
2021-09-01
Completion
2021-10-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04331210 on ClinicalTrials.gov