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Clinical Trials/IRCT20120915010841N10
IRCT20120915010841N10
Recruiting
Phase 2

Comparison of intra techal injection of fentanyl and sufentanil on the onset, duration and quality of analgesia in vaginal delivery under spinal anesthesia .

Hamedan University of Medical Sciences0 sites50 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Vaginal delivery under spinal analgesia.
Sponsor
Hamedan University of Medical Sciences
Enrollment
50
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients with class 1 and 2 of physical status(ASA)
  • The second pregnancy
  • Gestational age 36 to 40 weeks
  • Aged 18 to 45 years old
  • Active phase of labor(Cervical dilatation is more than 5 cm)

Exclusion Criteria

  • Heart disease
  • Spinal anesthesia Contraindication(High ICP, coagulation problems, shock, anemia)
  • History of opioid use in 24 hours before delivery

Outcomes

Primary Outcomes

Not specified

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