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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03694873
Other study ID # perineal pain
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date October 10, 2018
Est. completion date December 10, 2018

Study information

Verified date October 2018
Source Cairo University
Contact AHMED SAMY, MD
Phone 01100681167
Email ahmedsamy8233@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial will be performed to compare the effectiveness of oral tramadol versus oral celecoxib for the management of perineal pain following episiotomy or perineal tear repair after spontaneous vaginal birth in obese women


Description:

Pain after episiotomy or tear of perineal tissues during childbirth is often inadequately treated and may be severe. Not only did perineal pain negatively affect the physical and mental functioning of the woman, but also it might decrease the success of breastfeeding and reduced her ability to care for her child. The methods of relieving perineal pain included medication and non-medication. When the perineal pain was mild, the most common analgesic used was acetaminophen. Whereas the perineal pain was more severe, other drugs had been chosen such as opioid, non-opioid, and a combination of both opioid and non-opioid analgesics


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 10, 2018
Est. primary completion date December 5, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Age:18-35 years

- Obese women with BMI = 30.

- completed full 37-weeks gestation.

- spontaneous vaginal delivery with medio-lateral episiotomy or perineal tear requiring repair.

- Singleton alive fetus.

Exclusion Criteria:

- known allergy to investigated drugs(tramadol or celecoxib).

- regular use of analgesic drugs before or during pregnancy.

- any medical condition known to be potentially exacerbated by opioids, including alimentary canal disorders, hepatic and renal disease.

- instrumental vaginal delivery.

- 3rd or 4th degree perineal tear.

- severe postpartum haemorrhage (>1,500 ml).

- complicating maternal diseases (pregestational/gestational diabetes mellitus; bleeding disorders; pre-eclampsia and other hypertensive disorders of pregnancy).

- epidural nor combined spinal-epidural analgesia in labour

- a history of peptic ulcer,asthma,thrombocytopaenia.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tramadol Hydrochloride
one tablet of Tramadol 100 mg (Tramaw, Global Napi, Giza,Egypt) administered orally immediately, 12 h and 24 h after randomization.
Celecoxib 200mg
Celecoxib 200 mg (Celebrex® 200, P?zer,USA) administered orally immediately, 12 h and 24 h after randomization.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary perineal pain perineal pain severity using visual analogue scale 1 hour after repair of episiotomy
Secondary perineal pain perineal pain severity using visual analogue scale 1 hours after repair of episiotomy
See also
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Terminated NCT04016467 - Effect of Spinal Manipulation on Vulvar Pain N/A
Not yet recruiting NCT06407505 - The Effect of LI4 Acupressure on Perineal Pain and Postpartum Comfort During Episiotomy Repair N/A
Recruiting NCT02024256 - Cold Magnesium Sulfate Solution for Perineal Swelling Following Vaginal Delivery N/A
Not yet recruiting NCT06008899 - Efficacy of Ultrasound-assisted Caudal Epidural Pulsed Radiofrequency for Anal Pain in Cancer Patients, N/A
Completed NCT05486624 - The Effect of Reiki Application on Episiotomy and Perineal Pain N/A