The Association Between Epidural Labor Analgesia and Pregnancy Outcomes

Sponsor
Deng Dongrui (Other)
Overall Status
Unknown status
CT.gov ID
NCT03381495
Collaborator
(none)
200
1
2
19.5
10.2

Study Details

Study Description

Brief Summary

Labor analgesia can alleviate intrapartum pain, in the importance of the delivery is very obvious.But some researches think labor analgesia may affect the progress of labor, increase the cesarean section rate.This research adopts the epidural anesthesia to study labor analgesia effects on delivery outcomes and long-term emotional and psychological effects on the mothers. Besides, we also want to study the effect of exercise during pregnancy on the mode of delivery.

Condition or Disease Intervention/Treatment Phase
  • Drug: Ropivacaine Hydrochloride, Sufentanil
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Association Between Epidural Labor Analgesia and Pregnancy Outcomes
Actual Study Start Date :
May 16, 2018
Anticipated Primary Completion Date :
Sep 1, 2018
Anticipated Study Completion Date :
Dec 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Epidural analgesia during labor

The epidural analgesia technique was used to maintain analgesia for parturients who request labor analgesia.First, we injected a test dose of 5ml 1% lidocaine . If not adverse effects were observed 10 minutes after the test dose, the parturient then received a bolus injection of an initial dose of 8-10 ml mixed liquids of 0.075% ropivacaine and 0.2ug/ml sufentanil citrate. We then connected the epidural catheter with a patient-controlled epidural analgesia (PCA) pump, which provided patients the same mixed solution at 8-10ml/h until the delivery of neonates.

Drug: Ropivacaine Hydrochloride, Sufentanil
In this research one group will receive epidural analgesia(Ropivacaine Hydrochloride, Sufentanil), data will be collected and analyzed between this group and non-epidural analgesia group.

No Intervention: Non-epidural analgesia during labor

Women who refused epidural labor analgesia were included in the non-epidural analgesia group, and they don't receive epidural analgesia during labor

Outcome Measures

Primary Outcome Measures

  1. Labor duration [At the end of the delivery]

    Duration of three stages of labor.

Secondary Outcome Measures

  1. 1 minute Apgar index [1 minute after the infant is born]

    The index indicates the infant s' conditions, including heart rate, breathing, muscle tone, reflex response, color. Each characteristic is given an individual score; two points for each of the five categories if all is completely well; then all scores are totaled. The score is from 0 to 10.

  2. 5 minute Apgar index [5 minutes after the infant is born]

    The index indicates the infant s' conditions, including heart rate, breathing, muscle tone, reflex response, color. Each characteristic is given an individual score; two points for each of the five categories if all is completely well; then all scores are totaled. The score is from 0 to 10.

  3. Visual Analogue Scores(VAS) [5min before analgesia;5min,15min, 30min,60min after analgesia; at the time of latent phase, active phase, full dilation of the cervix, crowning of head, and laceration repair.]

    VAS is the most common pain scale for quantification. The score is from 0 to 10. The score is higher, the patient will be more painful. That will indicate if the analgesia is effective.

  4. Modified Bromage scores [5min before analgesia;5min,15min, 30min,60min after analgesia; at the time of latent phase, active phase, full dilation of the cervix, crowning of head, and laceration repair.]

    The modified Bromage score is the most frequently used measure of motor block. The scores is from 0 to 3. In this scale, the intensity of motor block is assessed by the patient's ability to move their lower extremities (0: no motor paralysis; 1: inability to raise extended leg, but able to move knee and foot; 2: inability to raise extended leg and to move knee, but able to move foot; 3: inability to raise extended leg or to move knee and foot). That will indicate if the analgesia block the patient motor too much.

  5. Postpartum depression [3 days after delivery,6 weeks after delivery, 3 months after delivery, 6 months after delivery, 1 year after delivery.]

    Assess the risk of postpartum depression among all participants using EPDS,HAMA.

  6. The mode of delivery [At the end of delivery]

    Including spontaneous vaginal delivery, vacuum- and forceps-assisted delivery, cesarean delivery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

healthy and full term pregnant women

Exclusion Criteria:

the pregnant women with complications

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei China 430030

Sponsors and Collaborators

  • Deng Dongrui

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Deng Dongrui, professor,chief doctor, Tongji Hospital
ClinicalTrials.gov Identifier:
NCT03381495
Other Study ID Numbers:
  • TJ-C20171201
First Posted:
Dec 22, 2017
Last Update Posted:
Jul 13, 2018
Last Verified:
Jul 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Deng Dongrui, professor,chief doctor, Tongji Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 13, 2018