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A Study for Assessing the Expected and Actual Pain of Back Injection in Pregnant Women Undergoing Caesarean Delivery

A Cross-Sectional Study to Evaluate the Anticipated and Experienced Pain at the Site of Spinal Needle Insertion in Patients Undergoing Elective Lower Segment Caesarean Section - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/01/078959
Enrollment
40
Registered
2025-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

SRM Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant Women ASA PS Grade 2 and 3 Elective Caesarean Section

Exclusion criteria

Exclusion criteria: Patient Refusal Contraindications for spinal anaesthesia Inability to comprehend information Previous history of chronic lower back pain Previous spinal anaesthesia experience More than 2 attempts for spinal anaesthesia Spinal conduct duration more than 20 minutes Cutting spinal needle more than 25G size

Design outcomes

Primary

MeasureTime frame
To assess the anticipated and experienced pain at the site of spinal needle insertionTimepoint: The day before surgery, and after spinal needle insertion—

Secondary

MeasureTime frame
To find out the anxiety associated with painTimepoint: Day before surgery;Number of attempts needed for spinal anaesthesiaTimepoint: At time of giving spinal anaesthesia;Time taken for spinal anaesthesiaTimepoint: Immediately after drug is given in spinal needle;To correlate the associated anxiety with the anticipated painTimepoint: After collection of data—

Countries

India

Contacts

Public ContactDr Swetha Ramani C

SRM Medical College Hospital and Research Centre

swethark@srmist.edu.in9884782554

Outcome results

None listed

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