FindTrial
Sign In

A study to compare two different doses of clonidine when added to ropivacaine in an ultrasound-guided abdominal nerve block (Transversus Abdominis Plane Block) for relieving pain after caesarean delivery

Comparison of two different doses of clonidine as adjuvant to ropivacaine in ultrasound guided transversus abdominis plane block for post caesarean analgesia?A prospective double blinded randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093582
Enrollment
90
Registered
2025-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: - Health Condition 2: - Health Condition 3: O749- Complication of anesthesia duringlabor and delivery, unspecified

Interventions

Intervention1: Comparison of two different doses of clonidine as adjuvant to ropivacaine in ultrasound guided transversus abdominis plane block for post caesarean analgesia?A prospective double blinde

Sponsors

Mirthan Krish B
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients belonging to American Society of Anaesthesiologist grade II posted for both elective and emergency lower segment caesarean section under Spinal?Anaesthesia

Exclusion criteria

Exclusion criteria: Patient not willing to participate in the study. Allergic to local anaesthetic agent. Patient BMI more than 30 kg per m2. Height less than 145cm. Contraindications to Spinal Anaesthesia (Coagulopathies, local?infections)

Design outcomes

Primary

MeasureTime frame
Duration of analgesic effects: It is noted considering the time of completion of the respective block procedure (I.E deposition of the required amount of local anaesthetic drug in to the desired plane) on each side as the reference point to the first rescue?analgesia.Timepoint: 0mins,30mins,1hour,4hours,8hours,12hours,24hours—

Secondary

MeasureTime frame
Time for first rescue analgesia and Comparing pain scores using visual analogue scale.Timepoint: 0mins,30mins,1hour,4hours,8hours,12hours,24hours—

Countries

India

Contacts

Public ContactMirthan krish B

Sri Venkateshwaraa medical college hospital and research?center

dr.jayashridevi@gmail.com8754689690

Outcome results

None listed

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