Trial · NCT02264834
Deambulatory Epidural During the Labour
NCT02264834, Phase 3, Completed, Dr Madeleine Wilwerth
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Deambulatory Epidural During the Labour. Trials, record NCT02264834. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02264834
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Deambulatory Epidural During the Labour
- NCT number
- NCT02264834
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 164 participants, actual
- Lead sponsor
- Dr Madeleine Wilwerth
- Conditions
- First Pregnancy
- Interventions
- Levobupivacaine 0.1% + Sufentanil 0.2µg/ml, Levobupivacaine 0.07% + Sufentanil 0.3µg/ml, Lumbar epidural analgesia
- First posted
- 2014-10-15
- Last updated
- 2018-05-31
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time between peridural application and childbirth | at delivery | This will be used to assess labor. |
| Primary | Caesarian | at delivery | This will be used to assess labor. Was a caesarian necessary (yes-no) ? |
| Primary | Instrumentalisation | at delivery | This will be used to assess labor. Was an instrumentalisation (defined as the use of forceps or suction cups) necessary at delivery (yes-no) ? |
| Primary | Apgar score of the baby | at delivery | Evaluation of the baby, using the Apgar score. This will be used to assess labor. |
| Secondary | Bromage score | 1h after the start of the peridural | Modified Bromage score (Breen et al) \>5 and ability to stand on one leg alternatively. This will be used to assess perambulation (motricity). |
| Secondary | Romberg test | 1h after the start of the peridural | Romberg test during 20-30 seconds. This will be used to assess perambulation (proprioception). |
| Secondary | Arterial tension | 1h after the start of the peridural | Absence of orthostatic hypotension (i-e less than 20% of the usual arterial tension of the patient). |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02264834
GET https://conductscience.org/api/trials/v1/NCT02264834/registered