Simple gel may speed up childbirth and reduce tears
NCT ID NCT07428317
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether applying a sterile lubricant gel during the pushing phase of labor can shorten delivery time and protect the mother's perineum. Researchers will compare 160 women who receive the gel to those who do not. The goal is to see if reducing friction helps the baby descend more easily, potentially lowering the need for episiotomies and reducing complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Obstetric lubricant gel
- What this could lead to
- If it works, this simple gel could make labor faster and safer for mothers, reducing the need for cuts or stitches.
- What could go wrong
- This is a small, early-stage study. The gel may not shorten labor or could cause irritation. Results may not apply to all pregnancies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 49 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed informed consent form * Willingness to comply with study procedures * Age between 18 and 40 years * Term pregnancy (37-41.6 weeks) with active labor * Diagnosis of spontaneous labor and planned vaginal delivery * Fetus in cephalic presentation * Agreement to comply with lifestyle restrictions during the study Exclusion Criteria: * Multiple pregnancy * Previous cesarean section * High-risk pregnancy (preeclampsia, uncontrolled gestational diabetes, etc.) * Presence of fever or active infection * Contraindication for vaginal delivery * Refusal to sign informed consent * Premature rupture of membranes \>18 hours without labor * Known allergy to lubricant gel components * Participation in another clinical trial in the last 3 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Escuela
RECRUITINGTegucigalpa, Francisco Morazán Department, 11101, Honduras