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Pentazocine With Rectal Diclofenac Versus Pentazocine Alone for Pain Relief Following Caesarean Delivery: A Randomised Controlled Trial

Not Applicable
Conditions
Caesarean Delivery
Registration Number
PACTR202107706925314
Lead Sponsor
Ofor Ifeanyichukwu
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
200
Inclusion Criteria

All consenting women with lower segment caesarean delivery under spinal anaesthesia
Women with term gestations (37-42 weeks)
Women with singleton pregnancy

Exclusion Criteria

Women with known history of peptic ulcer disease
Women with allergies to NSAIDs and pentazocine
Sickle cell disease patients
Asthmatic patients
Patients who had still births
Patients with opiod dependency
Obese women
Patients who had still births
Patients with morbidities that may affect pain management
Patients who may have complicated and prolonged surgeries (lasting over 90 minutes)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The level of pain perception measured using the VAS for pain.
Secondary Outcome Measures
NameTimeMethod
evel of satisfaction with pain relief, ;Need for breakthrough analgesia;Maternal side effects;Time of onset of bowel movement;Time of onset of ambulation
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