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A Comparative Study Of Two Drugs in patients with history of Scorpion Bite Posted For Below Umbilical Surgery

An Observational Study To Compare Effectiveness Between Intra-thecal Hyperbaric Bupivacaine 0.5% Versus Hyperbaric Ropivacaine 0.5% In Patients With History Of Scorpion Bite Posted For Below Umbilical Surgery Under Spinal Anaesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084575
Enrollment
276
Registered
2025-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Control Intervention1: Injection Bupivacaine Heavy 0.5%: This is most commonly used anaesthetic agent for Spinal Anaethesia. Control Intervention2: Injection Ropivacaine Heavy 0.5%: this is comparativ

Sponsors

SBKS MEDICAL INSTITUTE AND RESEARCH CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. PATIENT WILLING TO SIGN THE INFORMED WRITTEN CONSENT 2. PATIENT OF ASA GRADE 1 AND 2 OF EITHER GENDER 3. UNDER SPINAL ANAESTHESIA FOR ELECTIVE PELVIC AND LOWER LIMB SURGERIES 4. AGED 20-60 YEARS 5. PATIENTS HAVING HISTORY OF SCORPION BITE 6. NO KNOWN HISTORY OF ALLERGY, SENSITIVITY TO LOCAL ANAESTHETICS OF THE AMIDE GROUP AND OTHER DRUGS USED FOR THIS STUDY 5 PATIENTS

Exclusion criteria

Exclusion criteria: 1.PATIENT REFUSAL 2.PATIENT NOT NIL BY MOUTH 3.HISTORY OF SEIZURE DISORDER 4.KNOWN ALLERGY TO TRIAL DRUGS 5.PATIENTS WITH NEUROLOGICAL DISORDERS AND NEUROPATHIES OR RECEIVING MEDICATIONS KNOWN TO INFLUENCE NEUROMUSCULAR JUNCTIONS 6.PATIENTS OF ASA GRADE 3, 4 AND 5 7.PREGNANT FEMALES 8.FAILED SPINAL ANAESTHESIA CONVERTED TO GENERAL ANAESTHESIA 9.ANY CONTRAINDICATION TO SPINAL ANAESTHESIA

Design outcomes

Primary

MeasureTime frame
TO COMPARE EFFICACY OF BUPIVACAINE AND ROPIVACAINE IN PATIENTS WITH HISTORY OF SCORPION BITETimepoint: AT 2 MINUTES, 5 MINUTES, 10 MINUTES, 15 MINUTES THEN EVERY 5 MINUTES FOR FIRST HOUR THEN AFTER EVERY 30 MINUTES TILL 2 LEVEL REGRESSION OF SENSORY BLOCKADE AND COMPLETE MOTOR REVERSAL—

Secondary

MeasureTime frame
ASSESMENT OF ONSET OF SENSORY AND MOTOR BLOCKADE, HIGHEST LEVEL AND DURATION Timepoint: AT 2 MINUTES, 5 MINUTES, 10 MINUTES, 15 MINUTES THEN EVERY 5 MINUTES FOR FIRST HOUR THEN AFTER EVERY 30 MINUTES TILL 2 LEVEL REGRESSION OF SENSORY BLOCKADE AND COMPLETE MOTOR REVERSAL—

Countries

India

Contacts

Public ContactDR ARPIT SHAH

SBKS MEDICAL INSTITUTE AND RESEARCH CENTRE

drarpitshah21@gmail.com8200278150

Outcome results

None listed

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