Trial · NCT02179294
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The proportion of women who receive epidural analgesia for pain relief in labour, in each group, after randomisation. | At labour | The proportion of women who receive epidural analgesia for pain relief in labour, in each group, after randomization. |
| Secondary | • The effectiveness of pain relief provided by each technique, quantified by Visual Analogue Scale | Post natally - Average of 2-3days after delivery | • The effectiveness of pain relief provided by each technique, quantified by Visual Analogue Scale |
| Secondary | The incidence of maternal side effects | Post Natally - Average of 2-3days after delivery | The incidence of maternal side effects including * Excessive sedation score * Oxygen Saturation \<94% whilst breathing room air * Nausea requiring anti-emetic administration * Requirement and indication for supplemental oxygen * Respiratory Depression (Respiratory rate \< 8 breaths/minute) |
| Secondary | Delivery mode (Spontaneous, Instrumental Vaginal, Caesarean Section) | Post Natally - Average of 2-3days after delivery | Delivery mode (Spontaneous, Instrumental Vaginal, Caesarean Section) |
| Secondary | Incidence of foetal distress requiring delivery | Post Natally - Average of 2-3days after delivery | Incidence of foetal distress requiring delivery |
| Secondary | Neonatal status at delivery | Post Natally - Average of 2-3days after delivery | Neonatal status at delivery: * Apgar score at 5 minutes * Incidence of foetal acidosis determined by umbilical cord gas analysis * Requirement for neonatal resuscitation * Incidence of and indication for admission to neonatal care |
| Secondary | Rate of initiation of breast feeding within the first hour of birth | Post Natally - 1 hour after delivery | Rate of initiation of breast feeding within the first hour of birth |
| Secondary | Maternal satisfaction with childbirth experience determined by postpartum questionnaire prior to discharge from the delivery ward | Post Natally - Average of 2-3days after delivery | Maternal satisfaction with childbirth experience determined by postpartum questionnaire prior to discharge from the delivery ward |
| Secondary | Maternal birth experience determined by qualitative telephone interview up to six weeks postpartum | Up to 6 weeks post-partum | Explore and compare women's birth experiences up to six weeks postpartum via qualitative telephone interview (Post-Natal sub-study) |
| Secondary | Maternal perceptions of pain relief determined by qualitative telephone interview up to six weeks postpartum | Up to 6 weeks post-partum | Explore and compare women's perceptions of pain relief up to six weeks postpartum via qualitative telephone interview (Post-Natal sub-study) |
| Secondary | Infant feeding behaviours determined by qualitative telephone interview up to six weeks postpartum | Up to 6 weeks post-partum | Explore and compare infant feeding behaviours up to six weeks postpartum via qualitative telephone interview (Post-Natal sub-study) |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02179294/registered