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Clinical Trials/CTRI/2013/02/003392
CTRI/2013/02/003392
Completed
Phase 4

A comparative study to evaluate the analgesic efficacy of Flupirtine maleate versus Ibuprofen in gynecological ambulatory surgeries - None

Department of Science and Technology0 sites60 target enrollmentTBD
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ConditionsHealth Condition 1: null- Females 18-70 years Gynecological ambulatory surgeries ranging up to 60 minutesHealth Condition 2: N958- Other specified menopausal and perimenopausal disorders

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: null- Females 18-70 years Gynecological ambulatory surgeries ranging up to 60 minutesHealth Condition 2: N958- Other specified menopausal and perimenopausal disorders
Sponsor
Department of Science and Technology
Enrollment
60
Status
Completed
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

Eligibility Criteria

Inclusion Criteria

  • •18\-70 years
  • •Body Mass Index 25\-30 kg/m2
  • •Gynecological ambulatory surgeries ranging up to 60 minutes
  • •American Society of Anaesthesiologist I\-II

Exclusion Criteria

  • •History of intake of any analgesics in past three days
  • •Known hypersensitivity to any of the drug under study
  • •Hepatic insufficiency
  • •Patient with impaired renal function
  • •Coagulopathy
  • •Previous cerebral vascular accident history
  • •History of uncontrolled cardiopulmonary disease

Outcomes

Primary Outcomes

Not specified

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