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Clinical Trials/IRCT20120915010841N26
IRCT20120915010841N26
Not Yet Recruiting
Phase 2

Comparative evaluation of effect of General anesthesia, Spinal anesthesia and Paracervical block on pain, nausea, vomiting and analgesic requirements in diagnostic Hysteroscopy.

Hamedan University of Medical Sciences0 sites66 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hysteroscopic surgery under general anesthesia, spinal anesthesia or para cervical block.
Sponsor
Hamedan University of Medical Sciences
Enrollment
66
Status
Not Yet Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients 18 to 45 years
  • ASA class1\&2
  • Candidate for diagnostic hysteroscopic surgery
  • Satisfaction to participate in the study
  • Do not use analgesics for 24 hours before surgery
  • Absence of contraindications to spinal anesthesia and general anesthesia

Exclusion Criteria

  • History of allergies to local anesthetics and propofol
  • Cardiac,respiratory,renal and liver diseases
  • Candidate patients for myomectomy or polypectomy with resectoscope
  • Electrolyte disturbances (sodium, potassium and calcium
  • Uterine prolapse
  • History of previous cervical or hysteroscopic surgery
  • History of nausea and vomiting following previous anesthesia or history of motion sickness
  • Lack of patient cooperation after initial interventions
  • Coagulation disorders

Outcomes

Primary Outcomes

Not specified

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