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Rectal Versus Oral Diclofenac Sodium in Relieving Post Episiotomy Pain

Rectal Versus Oral Diclofenac Sodium in Relieving Post Episiotomy Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04331210
Enrollment
1024
Registered
2020-04-02
Start date
2020-09-01
Completion date
2021-10-01
Last updated
2020-04-02

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

Conditions

Episiotomy Wound

Keywords

Episiotomy

Brief summary

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

Detailed description

* Episiotomy is a surgical incision of the perineum and the posterior vaginal wall. * it can be done at a 60 degree angle from the vulva towards the anus or at an angle from the posterior end of the vulva. * usually under local anesthetic and is sutured after delivery. * It is done during second stage of labor to enlarge the opening for the baby to pass through to avoid soft-tissue tearing which may involve the anal sphincter and rectum. * Perineal pain after episiotomy has immediate and long-term negative effects for women and their babies. These effects can interfere with breastfeeding and the care of the infant. * Usually women undergo episiotomy need a good analgesic to overcome pain resulting from the analgesic. * Previous study by Faiza shafi, Shazia sayed, Naheed bano, Rizwana chaudhri, Holy family hospital, Rawalpindi, Pakistan, The study was published in journal of Rawalpindi medical college and concluded that rectal diclofenac should be further promoted , for pain relief, in women following episiotomy.

Interventions

DRUGDiclofenac Sodium

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

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

1. age: 20:35 years. 2. Primigravidae as elective procedure. 3. face to pubis delivery. 4. Big baby. 5. Narrow pelvic arch. 6. Elderly primigravida. 7. old perineal scar as episiotomy or perineorrhaphy. 8. Manipulative delivery. 9. To cut short second stage cases such as pre eclampsia. 10. Premature baby. 11. Fetal distress.

Exclusion criteria

1. more than 35 years. 2. pelvic inflammatory disease.

Design outcomes

Primary

MeasureTime frameDescription
Post episiotomy pain reliefFirst three days after deliveryThe relief of pain after delivery measured by pain relief scale..Pain relief scale Title: pain intensity scale Minimum 0 means no pain Maximum 4 means severe pain

Contacts

Primary ContactMohammed Hosny, Physician
Elto3my@yahoo.com01140762577

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026