FindTrial
Sign In

To test different concentrations of drug required to produce spinal anesthesia in urological surgery

Comparison Of Different Doses Of Hyperbaric Bupivacaine(0.5%) With Fentanyl For Elderly Patients Undergoing Endoscopic Urological Surgery Under Spinal Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039828
Enrollment
146
Registered
2022-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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: 7.5 mg of hyperbaric bupivacaine(0.5%) with 25 mcg of fentanyl under spinal anesthesia once.: 7.5 mg of hyperbaric bupivacaine with 25 mcg of fentanyl will be given as sub arachnid bloc

Sponsors

INDIRA GANDHI MEDICAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Surgery requiring level of T10 block as TURP/TURBT ASA CLASS I -III

Exclusion criteria

Exclusion criteria: Infection at site of block Patients where spinal anesthesia is contraindicated Coagulopathy Allergy Previous MI Pulmonary disease Anatomical deformity of spine

Design outcomes

Primary

MeasureTime frame
To compare hemodynamic parameters amongst groupsTimepoint: Heart rate, spo2, MAP monitoring at 2 min interval from time of injectio for 20 minutes,thereafter 5 minutes intervals,for 30 minutes from injection time till 30 minutes of complete resolution of sensory and motor blockade—

Secondary

MeasureTime frame
To see the onset and duration of sensory and motor blockade achieved in patients To see side effects of any.Timepoint: Time at which spinal anesthesia is given, onset of sensory block,time to complete sensory regression , time to complete motor regression,—

Countries

India

Contacts

Public ContactNeha Atwal

Professor

aparnasharmaraina@gmail.com9418083224

Outcome results

None listed

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