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Clinical Trials/CTRI/2023/04/051776
CTRI/2023/04/051776
Not Yet Recruiting
Phase 3

A prospective, interventional study to evaluate the effect of epidural volume extension on the characteristics of subarachnoid block with low dose of hyperbaric bupivacaine in patients undergoing infraumbilical surgeries

ESIC Medical College and Hospital0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: I839- Asymptomatic varicose veins of lower extremitiesHealth Condition 2: S720- Fracture of head and neck of femurHealth Condition 3: R103- Pain localized to other parts of lower abdomen
Sponsor
ESIC Medical College and Hospital
Status
Not Yet Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
ESIC Medical College and Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\. American Society of Anesthesiologists (ASA) status Iâ??II
  • 2\. Belonging to both genders
  • 3\. Age \- 18 years to 60 years
  • 4\. Type of Surgery â??Elective Infraumbilical surgeries under CSE
  • 5\. Valid written informed consent

Exclusion Criteria

  • 1\. ASA • \& â?£
  • 2\. BMI \> 30kg/m2
  • 3\. Height \- \< 150cm
  • 4\. Patients with a history of spinal disease/deformities
  • 5\. Coagulation abnormality
  • 6\. Sensitivity to bupivacaine
  • 7\. Contraindications to central neuraxial block
  • 8\. Local infections
  • 9\. Patient refusal
  • Post inclusion exclusion criteria: Patients with inadequate block who require epidural top ups with local anaesthetic at any time during the surgery

Outcomes

Primary Outcomes

Not specified

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