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Comparison between hyperbaric Ropivacaine and hyperbaric Bupivacaine in patients undergoing inguinal and perineal surgeries under spinal anaesthesia.

A Comparative evaluation of Hyperbaric Ropivacaine versus Hyperbaric Bupivacaine for elective Inguinal and Perineal surgery under spinal anaesthesia.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/050035
Enrollment
30
Registered
2023-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: Injection ropivacaine heavy: Dose 30mg intrathecal route. Duration 20 minutes post spinal anesthesia We observe for onset, duration, extend and recovery time of sensory block (analges

Sponsors

Dr D Y Patil Medical college Hospital and Research Centre Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing inguinal and perineal surgeries under spinal anesthesia. 2. Hemodynamically stable patients with all routine investigations within normal limits with no co-morbidities. 3. Patients who are not on any cardiac related drugs. 4. Availability of informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with ASA physical status 3 or more. 2. Patients below 18 years and above 60 years of age. 3. Patients posted for emergency procedures. 4. Patients with major neurological, cardiac, respiratory, metabolic, renal, hepatic disease or any coagulation abnormalities. 5. Patients contraindicated for spinal anesthesia. 6. Patients with known allergies to the study drugs.

Design outcomes

Primary

MeasureTime frame
Time taken for the onset of sensory block followed by Time taken to T8 level sensory blockade post subarachnoid block with either injection bupivacaine heavy or injection ropivacaine heavy. Timepoint: 2 minutes to 15 minutes

Secondary

MeasureTime frame
5. To observe for any incidence of adverse events and for the need of general anesthesia (GA) supplementation.Timepoint: 2 to 20 minutes;Duration of sensory blockadeTimepoint: 150 minutes;Intraoperative hemodynamic parameters like heart rate, blood pressureTimepoint: 2 minutes to 150 minutes;Onset and duration of motor blockadeTimepoint: 2 minutes to 150 minutes;Time of first micuritionTimepoint: At 120 to 150 minutes post subarachnoid block

Countries

India

Contacts

Public ContactDr Dipanjali Mahanta

Dr. D Y Patil Vidyapeeth

dipanjalimahanta@gmail.com09673586122

Outcome results

None listed

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