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"A Randomized Study Comparing Ropivacaine and Bupivacaine with Fentanyl for Lower Abdominal Surgeries: Effects on Pain Management and Patient Outcomes."

Comparison of Isobaric 0.75 Ropivacaine with fentanyl versus Hyperbaric 0.5 Bupivacaine with fentanyl in Spinal anaesthesia for infraumbilical surgeries. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074657
Enrollment
100
Registered
2024-10-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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: Ropivacaine isobaric: Group A will receive a single intrathecal administration of isobaric 0.75% ropivacaine combined with fentanyl just before the surgical procedure. Control Intervent

Sponsors

Dr Deepak R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Elective infraumbilical surgical procedures 2. Surgeries performed under spinal anesthesia 3. Surgical duration anticipated to be within 2 hours 30 minutes.

Exclusion criteria

Exclusion criteria: 1. Patients with bleeding disorders 2. ASA III and IV patients

Design outcomes

Primary

MeasureTime frame
To compare the hemodynamic changes associated with isobaric 0.75% ropivacaine with fentanyl versus hyperbaric 0.5% bupivacaine with fentanyl during spinal anesthesia for infraumbilical surgery.Timepoint: Before Induction, During Induction, 3 minutes, 6 minutes, 9 minutes, 12 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 45 minutes, 60 minutes, 75 minutes, 90 minutes, 105 minutes, 120 minutes, 135 minutes, 150 minutes, 165 minutes, 180 minutes.

Secondary

MeasureTime frame
1. To compare the duration of onset of sensory and motor blockade between the two anesthetic combinations. 2. To assess the quality of sensory and motor blockade provided by each anesthetic regimen. 3. To evaluate the incidence and nature of adverse drug reactions associated with each anesthetic combination. Timepoint: Before Induction, During Induction, 3 minutes, 6 minutes, 9 minutes, 12 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 45 minutes, 60 minutes, 75 minutes, 90 minutes, 105 minutes, 120 minutes, 135 minutes, 150 minutes, 165 minutes, 180 minutes.

Countries

India

Contacts

Public ContactDr Deepak R

BJ govt medical college, Pune

deepaknr0609@gmail.com8983741147

Outcome results

None listed

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