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Comparision of Hyperbaric Ropivacaine Alone or with Fentanyl in Spinal Anaesthesia for Abdominal Hysterectomy

Clinical Efficacy of Hyperbaric Ropivacaine 0.75% Alone or with Fentanyl in Spinal Anaesthesia for Abdominal Hysterectomy; a Prospective Randomised Double Blind Study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067077
Enrollment
80
Registered
2024-05-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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: Spinal Anaesthesia: Duration of analgesia is compared between Hyperbaric Ropivacaine 0.75 percentage (18.75 mg) with Fentanyl (25 microgram)or Hyperbaric Ropivacaine 0.75 percentage

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with American Society of Anesthesiologists physical status I-II, Scheduled for elective abdominal hysterectomy under Spinal Anaesthesia, Height = 140cm, Weight: 40kg - 65kg

Exclusion criteria

Exclusion criteria: Patient refusal, Patient with Coagulopathies or on anticoagulant medication, any specific disease with absolute contraindications of Spinal Anaesthesia, hypothyroidism or diabetic neuropathy and Psychiatric disorder / disease and history of allergic reaction to study drugs.

Design outcomes

Primary

MeasureTime frame
Increase In The Duration Of Post Operative AnalgesiaTimepoint: 0 hour,0.5 hour, 1 hour, 1.5 hour,2 hour,2.5 hour,3 hour, 3.5 hour, 4 hour, 4.5 hour, 5 hour

Secondary

MeasureTime frame
Total Duration Of Sensory Block & Total Duration Of Motor BlockTimepoint: 0 hour,0.5 hour, 1 hour, 1.5 hour,2 hour,2.5 hour,3 hour, 3.5 hour, 4 hour, 4.5 hour, 5 hour

Countries

India

Contacts

Public ContactRavindra Kumar Gehlot

R.N.T Medical College

dr.rgehlot.2010@gmail.com9468694902

Outcome results

None listed

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