Postoperative Pain Clinical Trial
Official title:
Does Bupivacaine Infiltration Reduce Postoperative Pain in Patients With Cesarean Section?
This is a double-blind randomized controlled trial to assess the efficacy of local infiltration of bupivacaine versus placebo, in reducing postoperative pain. The severity of pain will be assessed in terms of mean score on visual analogue scale, opioid requirement and average duration of hospital stay.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | April 10, 2021 |
Est. primary completion date | April 10, 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 40 Years |
Eligibility | Inclusion Criteria: - pregnant women with age between 20-40 years, American Society of Anesthesiologist (ASA) class II, BMI < 35 at the time of surgery, a period of gestation 37+0- 40+0 weeks, elective caesarean section done under spinal anesthesia, skin incision pfennensteil and lower segment transverse incision on the uterus. Exclusion Criteria: - allergy to local anesthetic, emergency caesarean section, conversion of spinal anesthesia to general anesthesia, caesarean section due to abnormal placentation, midline skin incision, upper segment incision on uterus |
Country | Name | City | State |
---|---|---|---|
Pakistan | Madiha Ahmed | Islamabad |
Lead Sponsor | Collaborator |
---|---|
Armed Forces Hospital, Pakistan |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | average pain score on Visual analogue scale | average pain score on Visual analogue scale in first 12 hours after the surgery | in first 12 hours after the surgery | |
Primary | average opioid consumption | average consumption of tramadol injection | within first 24 hours after the surgery | |
Secondary | average duration of hospital stay | average duration of hospital stay after the surgery | 3 months |
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