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COMPARATIVE STUDY OF HYPERBARIC ROPIVACAINE (0.75%) AND HYPERBARIC BUPIVACAINE (0.5%) FOR DAY CARE PERINEAL SURGERIES UNDER SPINAL ANAESTHESIA

COMPARATIVE STUDY OF INTRATHECAL HYPERBARIC ROPIVACAINE (0.75%) AND HYPERBARIC BUPIVACAINE (0.5%) FOR DAY CARE PERINEAL SURGERIES UNDER SUBARACHNOID BLOCK : A PROSPECTIVE RANDOMIZED DOUBLE-BLIND STUDY

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/051019
Enrollment
60
Registered
2023-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: 0.75% HYPERBARIC ROPIVACAINE: 2ML OF INTRATHECAL HYPERBARIC ROPIVACAINE (0.75%) IS ADMINISTERED UNDER SUBARACHNOID BLOCK FOR DAY CARE PERINEAL SURGERIES AND THE PATIENT IS MONITORED FOR

Sponsors

DR ASHOK KULASEKAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.American society of Anaesthesiologists(ASA) grade I-II, 2.Age group between 18-65 years of both sexes. 3. Scheduled for Perineal surgeries under spinal Anaesthesia with expected duration of surgery less than 90 minutes.

Exclusion criteria

Exclusion criteria: 1.Patient refusal 2.History of allergy to test drug 3.Post spinal surgeries, spinal deformities, skin sepsis in lumbar region, patient with pre-existing neurological disorders 4.coagulopathy 5.Dysrhythmia 6.Major Hepatic, renal and cardiovascular dysfunction. 7.BMI >35 8.Height 9.Surgeries involving major blood loss.

Design outcomes

Primary

MeasureTime frame
Duration of motor blockTimepoint: Patient is placed in sitting position for 15 minutes following the test drug administration via subarachnoid block .Duration of motor block will be assessed from baseline-15 minutes from the time of administering the test drug, and 20 minutes, followed by every 30 minutes interval upto 200 minutes.

Secondary

MeasureTime frame
Highest level of sensory blockTimepoint: Duration of sensory block will be assessed from baseline-15 minutes from the time of administering the test drug, and 20 minutes, followed by every 30 minutes interval upto 200 minutes.;To assess Hemodynamic changes and side effects, if anyTimepoint: Patients heart rate, NIBP, SPO2 will be monitored at 3 minute interval up to 15 minutes then every 5 minutes up to 60 minutes then every 10 minutes till the end of the procedure.

Countries

India

Contacts

Public ContactDR ASHOK KULASEKAR

CHETTINAD ACADEMY OF RESEARCH AND EDUCATION

ashokk_dr@yahoo.com9840498420

Outcome results

None listed

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