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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06089200
Other study ID # AN-202310.01
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date February 23, 2023
Est. completion date April 28, 2023

Study information

Verified date October 2023
Source Universitas Padjadjaran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized controlled trial is to compare the effect of TAP block vs spinal morphine for post caesarean section analgesics. The main questions it aims to answer are: - Which post op analgesic method works better for patients who underwent caesarean section - The number of additional opioid needed


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date April 28, 2023
Est. primary completion date April 28, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Indicated for caesarean section as assessed by Obstetricians - ASA II - Consented to be included in the study Exclusion Criteria: - Allergy history - Spinal converted to general anesthesia

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Transversus Abdominal Plane Block
20 cc of bupivacaine 0.2% was given to the transversus abdominis plane
Spinal Morphine
100 µg was administered intrathecally preoperatively

Locations

Country Name City State
Indonesia Hasan Sadikin General Hospital Bandung Jawa Barat

Sponsors (1)

Lead Sponsor Collaborator
Universitas Padjadjaran

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Length of time the patient needed the first additional opioid analgesics 24 hours post operative
Primary Total need for additional opioids 24 hours post operative
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