Comparison of ropivacaine with adjuvant(fentanyl) in spinal block in delivery by operation

Evaluation of anaesthetic effects of intrathecal hyperbaric Ropivacaine with or without fentanyl in lower segment caesarean section: a parallel group design, double blind, randomized control study. - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/09/057961

Enrollment

Registered

2023-09-22

Start date

Unknown

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery Health Condition 2: O- Medical and Surgical Health Condition 3: 1- Obstetrics

Interventions

Intervention1: Intrathecal ropivacaine with fentanyl: Hyperbaric ropivacaine 0.75% - 1.5ml (11.25mg) + Fentanyl 0.5ml (25mcg) Control Intervention1: Intrathecal ropivacaine with normal saline: Hyperba

Eligibility

Inclusion criteria

Inclusion criteria: 1. Parturients with ASA physical status grade II. 2. Posted for elective lower segment caesarean section under SAB.

Exclusion criteria

Exclusion criteria: 1. Parturient’s refusal to participate in study. 2. Parturients having coagulation abnormalities, platelet count 1.5, or on anticoagulants. 3. Parturients having systemic illness (like severe hypovolemia, raised intracranial pressure, neuromuscular diseases, ischemic/ valvular/ congenital heart diseases, psychiatric, hematological disorder). 4. Parturients having any absolute contraindications for spinal anaesthesia. 5. Any allergy to local anaesthetic. 6. Short stature (height 7. Morbid obesity (BMI > 40).

Design outcomes

Primary

Measure	Time frame
Duration of analgesia.Timepoint: Upto 6 hours post-operatively.	—

Secondary

Measure	Time frame
1. Sensory and motor block characteristics including onset, peak level and duration. 2. Haemodynamic parameters. 3. Adverse effects.Timepoint: Upto 24 hours post-operatively.	—

Countries

India

Contacts

Public ContactDr Gayatri Deshpande

RNT Medical College

htungaria@gmail.com9829370866

Outcome results

None listed

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