The Analgesic Effect of Butorphanol After Cesarean Section

Tongji Hospital

Status: Unknown

Conditions: Analgesia

Treatments: Drug: butorphanol

Study type: Interventional

Funder types: Other

Identifiers

NCT04490980

TJ-C20200119

Details and patient eligibility

About

We evaluated the clinical effect of Butorphanol on postoperative analgesia by observing the vital signs of patients, general condition of newborns and pain assessment.

Enrollment: 100 estimated patients

Sex: Female

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Healthy women at term (37 to 42 weeks of gestation), who desired cesarean section were eligible to participate. undergoing ；No drug sensitive history

Exclusion criteria

Patients with a history of anesthetics allergy and patients with preterm labor, multiple pregnancies and severe obstetric complications

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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100 participants in 2 patient groups

Observed group

Experimental group

Treatment:

Drug: butorphanol

Control group

No Intervention group