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Comparison of injecting bupivacaine in two different manners while giving spinal anaesthesia in abdominal hysterectomy

Comparison of fractionated dose versus bolus dose of injection bupivacaine in spinal anaesthesia for patients undergoing abdominal hysterectomy: A randomized double blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/023765
Enrollment
100
Registered
2020-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system Health Condition 2: N80-N98- Noninflammatory disorders of female genital tract

Interventions

Intervention1: Intrathecal block: Duration of study is around one year. Hemodynamic responses and duration of analgesia, characteristics of sensory and motor block are assessed Control Intervention1:

Sponsors

Jawahar Lal Nehru medical college Ajmer
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA grade 1 and 2 Patients giving valid informed consent

Exclusion criteria

Exclusion criteria: Patient refusal ASA grade 3 and above Cardiovascular or Cerebrovascular disease Diabetes and other associated illness Any contraindication to spinal anaesthesia

Design outcomes

Primary

MeasureTime frame
Hemodynamic responsesTimepoint: One year—

Secondary

MeasureTime frame
Duration of analgesia Characteristics of sensory and motor block Any significant side effects or complicationsTimepoint: One year—

Countries

India

Contacts

Public ContactDr Veena Patodi

Jawahar Lal Nehru medical college Ajmer

veenapatodi@gmail.com9414008276

Outcome results

None listed

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