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PARTICIPANTS ARE ELECTIVE GYNECOLOGICALPROCEDURES which will be done in spinal anaesthesia we used to compare two drug component one group will receive ropivacaine alone and another group will receive ropivacaine with adjuvant fentanyl ropivacaine is more cardiostable as compare to bupivacaine

A RANDOMISED CONTROLLED TRIAL TO COMPARE 0.75 PERCENTAGE HYPERBARIC ROPIVACAINE ALONE VERSUS 0.75 PERCENTAGE HYPERBARIC ROPIVACAINE WITH ADJUVANT FENTANYL FOR GYNECOLOGICAL SURGERIES UNDER SPINAL ANAESTHESIA - hyperbaric ropivacaine with adjuvant fentanyl versus hyperbaric ropivacaine alone in gynaecological surgeries

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086392
Enrollment
100
Registered
2025-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: N800- Endometriosis of uterus

Interventions

Intervention1: spinal anaesthesia in elective gynecological surgeries: spinal anaesthesia with two different drug group and compare 0.75% hyperbaric ropivacaine alone with 0.75% hyperbaric ropivacain

Sponsors

Dr Palak dineshbhai sitapara self
Lead Sponsor
Dr Divya Kheskani
Collaborator
Dr Heena Channwal
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: elective gynecological surgeries informed and written consent

Exclusion criteria

Exclusion criteria: refusal of patients local site lumbar infection spine deformities coagulopathies major systemic illness

Design outcomes

Primary

MeasureTime frame
to observe time to onset and duration of sensory and motor blockade NRS for post operative painTimepoint: after spinal anesthesia every 2 mins then every 5 min and every 19 min then every 30 mins and half hourly for 12 hours of spinal ananesthesia—

Secondary

MeasureTime frame
to observehemodynamics perioperative to observe duration of postoperative analgesia to observe perioperative any side effects & complicationsTimepoint: at baseline, every 5 mins then every 10 min,every 30 mins till 12 hours of spinal anaesthesia—

Countries

India

Contacts

Public ContactPalak dineshbhai sitapara

GCS medical college, hospital and research centre

palaksitapara@gmail.com9638037632

Outcome results

None listed

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