Trials / Unknown
UnknownNCT03622047
Comparison of Epidural Labor Analgesia With Dexmedetomidine or Sufentanil
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 1,800 (estimated)
- Sponsor
- Fudan University · Academic / Other
- Sex
- Female
- Age
- 22 Years – 42 Years
- Healthy volunteers
- Not accepted
Summary
The participants: 1800 full-term primiparas will be selected with ASA I-Ⅱgrade, 20 to 35 years old and weighing 55 to 90 kg in the investigator's hospital from may 2018 to December 2018. 1200 primiparas were divided into A and B according to the computer randomized numbers, and 600 parturients without labor analgesia in the same period were selected as group C, with 600 patients in each group. All parturients signed the informed consent form and were approved by the hospital ethics Committee.
Detailed description
1200 primiparas were divided into A and B according to the computer randomized numbers, and 600 parturients without labor analgesia in the same period were selected as group C, with 600 patients in each group. All parturients signed the informed consent form and were approved by the hospital ethics Committee.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexmedetomidine ropivacaine | Observing the effect of 0.5 μ g / ml sufentanil+ 0.1 % ropivacaine with 2 hours after fetal delivery, and the patients leave the delivery room without abnormality. |
| DRUG | No analgesia labor | No analgesia labor control group |
Timeline
- Start date
- 2018-08-15
- Primary completion
- 2020-08-01
- Completion
- 2020-08-01
- First posted
- 2018-08-09
- Last updated
- 2020-02-05
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03622047. Inclusion in this directory is not an endorsement.