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To compare spinal anesthesia using bupivacaine heavy (0.5%) with fentanyl to ropivacaine heavy (0.75%) with fentanyl in lower segment Cesarean section.

Compartive study of intrathecal hyperbaric ropivacaine (0.75%) with fentanyl versus hyperbaric bupivacaine (0.5%) with fentanyl in lower segment caesrean section- A prospective randomized double blind clinical study - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057213
Enrollment
40
Registered
2023-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O30-O48- Maternal care related to the fetus and amniotic cavity and possible delivery problems Health Condition 2: I95-I99- Other and unspecified disorders of the circulatory system Health Condition 3: O94-O9A- Other obstetric conditions, not elsewhere classified Health Condition 4: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Intrathecal hyperbaric ropivacaine (0.75%) with fentanyl 25 µg: Group RF- will receive 3ml of hyperbaric ropivacaine 0.75% plus 25ug fentanyl intrathecally and total duration of interve

Sponsors

Alok Kumar Bharti
Lead Sponsor
Mumtaz Hussain IGIMS Patna
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Full term pregnancy ASA I and II LSCS

Exclusion criteria

Exclusion criteria: patient refusal, having allergy to studied drugs, any contraindication to spinal anaesthesia, multiple pregnancies, suspected fetal abnormality or complicated pregnancies.

Design outcomes

Primary

MeasureTime frame
To assess Block characteristics objectively.Timepoint: Till sensory motor blockade achieved as per protocol

Secondary

MeasureTime frame
To assess hemodynamic parameter postoperative analgesia, time to first rescue side effectsTimepoint: till first rescue analgesia required;To assess hemodynamic parameter, duration of postop analgesia time to first rescue analgesia side effects seenTimepoint: Time to first rescue analgesia needed

Countries

India

Contacts

Public ContactDR ALOK KUMAR BHARTI

Indira Gandhi Institute of Medical Sciences, Patna

alok.bharti48@gmail.com09307645596

Outcome results

None listed

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