comparing the efficacy of inj. Bupivaccaine and inj. ropivaccaine as analgesia in cesarean section

Clinical Evaluation of Efficacy and Safety of Transversus Abdominis Plane Block with Inj. Levobupivacaine v/s Inj. Ropivacaine for Post Operative Analgesia following Lower Segment Cesarean Section: A Prospective, Randomised, Double Blind Study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/07/020098

Enrollment

Registered

2019-07-09

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Transversus Abdominis Plane Block with Inj. levobupivacaine v/s Inj. Ropivacaine after Lower Segmaent Cesarean Section: Clinical evaluation of efficacy and safety of trnasversus abdomin

Eligibility

Inclusion criteria

Inclusion criteria: 1. Informed written consent for participation in study. 2. Age: 20 to 35 years 3. Antenatal female patients scheduled for lower segment cesarean scetion. 4. Primi patients undergoing LSCS d/t CPD, Diabetes, Placenta Previa. 5. Singleton pregnancy 6. ASA physical status 1 and 2

Exclusion criteria

Exclusion criteria: 1. Patient refusing consent. 2. Multiple pregnancy 3. Mutipara 4. Neuropsychiatric disorder 5. Patient having post partum psychosis. 6. Allergy or hypersensitivity to local anesthetic or NSAIDS. 7. Anemia 8. Patient on any form of analgesics therapy. 9. Patient on ECG showing QT prolongtion. 10. ASA pysical status 3 and 4. 11. Contraindication to spinal anesthesia - Local infection or sepsis at site of Lumbar Puncture. - Bleeding disorders, thrombocytopenia - Space occupying lesons of the brain. - Anatomical disorder of spine - Hypovolemia e.g. following massive hemorrhage

Design outcomes

Primary

Measure	Time frame
-Visual Analogue Scale (VAS) -Patients satisfaction score -Surgeons satisfaction score -Total dose and frequency of rescue anlgesia.Timepoint: -30 min, 2,4,6,12,16,20,24	—

Secondary

Measure	Time frame
Effect on hemodynamic parmeters like heart rate, mean arterial pressure, oxygen saturation - side effects and comlications if anyTimepoint: 30 min, 2,4,6,12,16,20,24	—

Countries

India

Contacts

Public ContactDr Ravikumar M Parmar

Government Medical College, Bhavnagar

ravirajparmar1@gmail.com09099097807

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026