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Comparative study of fentanyl vs butorphanol in heavy levobupivacaine as a drug in spinal for pain relief in patients undergoing infra umbilical surgery

Comparative study of intrathecal fentanyl vs butorphanol along with heavy levobupivacaine for analgesic efficacy in adult patients undergoing elective infra umbilical surgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088008
Enrollment
180
Registered
2025-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: S70-S79- Injuries to the hip and thigh Health Condition 2: S80-S89- Injuries to the knee and lower leg Health Condition 3: S90-S99- Injuries to the ankle and foot Health Condition 4: M232- Derangement of meniscus due to oldtear or injury Health Condition 5: O- Medical and Surgical

Interventions

Intervention1: Intrathecal levobupivacaine with NS: To evaluate duration of sensory block with intrathecal 0.5percent levobupivacaine and 0.5ml Normal saline. Control Intervention1: Intrathecal Levobu

Sponsors

Dr Sarvjeet kaur
Lead Sponsor
Dr Haramritpal kaur
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either gender, aged between 18 and 65 years. 2. Patients of American Society of Anesthesiology Grade I and II physical status. 3. Patients scheduled for elective infraumbilical surgery under spinal anaesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with known allergy to any of the study drugs. 2. All known contraindications to spinal anaesthesia like: o Patients with coagulation disorders and on anticoagulants. o Patients with local skin infection or disease. o Patients with previous spinal surgeries, spine abnormalities. 3. Patient refusal.

Design outcomes

Primary

MeasureTime frame
To evaluate the duration of sensory and motor blockTimepoint: with in 24hrs postoperatively

Secondary

MeasureTime frame
Need for rescue analgesiaTimepoint: Till the effect of spinal analgesia subsides

Countries

India

Contacts

Public ContactDr Sarvjeet Kaur

Professor, Department of Anaesthesia

drsarvjeetk@gmail.com9915680508

Outcome results

None listed

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