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Clinical Trials/CTRI/2021/12/038876
CTRI/2021/12/038876
Not yet recruiting
未知

A Comparative study on the efficacy of Intrathecal 0.5% hyperbaric Bupivacaine with 20mcg Fentanyl in Single syringe versus Separate syringe techniques in Abdominal Hysterectomy

Mary Chacko0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: N859- Noninflammatory disorder of uterus, unspecified

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: N859- Noninflammatory disorder of uterus, unspecified
Sponsor
Mary Chacko
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Mary Chacko

Eligibility Criteria

Inclusion Criteria

  • •1\.ASA 1 and 2
  • •2\.Age between 30 and 65 year
  • •3\.Height between 150 and 180 cm
  • •4\.Body Weight between 45 and 75 kgs
  • •5\.Patients undergoing Elective Lower Abdominal Hysterectomy

Exclusion Criteria

  • •1\.ASA 3 AND 4
  • •2\.AGE \<30 YEAR AND \>65 YEAR
  • •3\.BODY WEIGHT \<45KG AND \>75KG
  • •4\.HEIGHT \<150CM AND \>180CM
  • •5\.MENTAL SUBNORMALITY
  • •6\.KNOWN ALLERGY TO DRUGS USED IN THE STUDY
  • •7\.NEUROLOGICAL OR NEUROMUSCULAR DISORDERS
  • •COAGULATION DISORDER
  • •8\.LOCAL INJECTION SITE INFECTIONS
  • •9\.PATIENT REFUSA

Outcomes

Primary Outcomes

Not specified

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