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A study to compare the anesthetic effects of different doses of spinal anaesthesia of inj. hyperbaric bupivacaine 0.5 percent for patients undergoing caesarean section

A prospective observational study to assess the anesthetic effects of different doses of intrathecal hyperbaric 0.5 percent bupivacaine for singleton caesarean section - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/077453
Enrollment
120
Registered
2024-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Control Intervention1: nil: nil

Sponsors

Dr Fulbestar Lyngdoh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pateints posted for singelton ceasarean section, belonging to Asa class I,II or III

Exclusion criteria

Exclusion criteria: Patients having major cardio pulmonary disorders or hepato renal disorders patients with multifetal pregnancy, hand or cord proplapse patients weight less than 40kgs or more than 90kgs patients height less then 140cm or more than 190cm

Design outcomes

Primary

MeasureTime frame
1. Motor and Sensory characteristics in all three groups 2. Hemodynamics parameters in all three groupsTimepoint: 1. Motor and Sensory characteristics in all three groups at the time of spinal anaesthesia upto the effects which weared off possibly between 1-4 hours 2. Hemodynamics parameters in all three groups after spinal anaesthesia—

Secondary

MeasureTime frame
1. Maternal satisfaction 2. Obsterics satisfactionTimepoint: baseline—

Countries

India

Contacts

Public ContactDr Sunaina Patel

Government Medical college, Surat

patel_sunaina@yahoo.com9825143013

Outcome results

None listed

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