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Rectal versus Oral Diclofenac for Relief of Perineal Pain after Episiotomy Repair: A Randomized Controlled Single-blind (Outcome Assessors) Study

Rectal versus Oral Diclofenac for Relief of Perineal Pain after Episiotomy Repair: A Randomized Controlled Single-blind (Outcome Assessors) Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202103495385214
Enrollment
176
Registered
2021-03-29
Start date
2021-05-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Pregnancy and Childbirth

Interventions

Sponsors

Dr. Ifeagwu Chika Sampson
Lead Sponsor
Dr. Adewole Adebayo Alade
Collaborator
Dr. Nzurumike Charles Nnanna
Collaborator
Dr. Musa Abdulkarim Omoyine
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Parturient with uncomplicated singleton pregnancy at term who will have episiotomy at delivery.

Exclusion criteria

Exclusion criteria: 1. Perineal tear other than episiotomy. 2. major postpartum haemorrhage. 3. History of NSAID allergy, gastric or duodenal ulcer, hepatic disease, renal disease, asthma, coagulopathy. 4. Any patient that will require special post-delivery pain control such as sickle cell disease patient and those who decline to be part of the study.

Design outcomes

Primary

MeasureTime frame
1. mean pain scores. 2. mean time interval between the first dose of both rectal or oral diclofenac and patient’s first demand for additional analgesia.

Secondary

MeasureTime frame
1. Proportion of women with side effects 2. Maternal satisfaction following rectal and oral diclofenac measured by Likert scale.

Countries

Nigeria

Contacts

Public ContactAdebayo;Chika Adewole;Ifeagwu

Consultant OBGYN Dept. of OBGYN Federal Medical Center Lokoja Nigeria. ;Senior Registrar Department of OBGYN Federal Medical Center Lokoja Nigeria

adewoleobsgyn@hotmail.com;scotoifeagwu@yahoo.com+2348036324806;+2348036694972

Outcome results

None listed

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