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Use of Acupuncture for Stimulation of Labour

Use of Acupuncture for Stimulation of Labour

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00279071
Enrollment
100
Registered
2006-01-19
Start date
2002-10-31
Completion date
2007-03-31
Last updated
2008-07-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dystocia

Keywords

dystocia, stimulation, acupuncture, oxytocin

Brief summary

Hypothesis:Acupuncture can be used as stimulation of labour in case of primary og secondary inertia. A randomized controlled trial including 150 pregnant women Acupuncture has become a natural part of the range of obstetric treatments offered in danish delivery wards, but there is only little evidence to the effect of the acupuncture. The women are randomized into to groups. 1. Acupuncture, Acu.points: KI3, Ki6, SP6, BL60, LI4, BL67(acupressure) 2. No treatment The women will be asked in case beginning signs of inertia, if they want to parcipitate in the trial. Inclusion criteria: 1. Normal pregnancy 2. In labour (orificium \< 8 cm), 37th week or thereafter 3. Ruptured membranes 4. Primary or secondary inertia The women will just before randomization be vaginally explored and fetal heart monitored. The meassure of effect happens two hours after randomization. The midwife who measures the effect, is blinded to the treatment or lack of, and also on the including exploration. Secondary effect meassures: length of labour, use of oxytocin and number of contracions pr/min meassured twice: 1\. before the randomization and again 1 hour after randomization.

Interventions

DEVICEAcupuncture og acupressure when diagnosed with dystocia

Acupuncture points: sp6 li4 ki3 ki6 bl60 Acupressure points: bl67

Sponsors

Ringkjøbing County Research Fond
CollaboratorUNKNOWN
Union of Midwives Research Fond
CollaboratorOTHER
Herning Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

1. Normal pregnancy 2. In labour (orificium \< 8 cm), 37th week or thereafter 3. Ruptured membranes 4. Primary or secondary inertia -

Exclusion criteria

1. Pathological pregnancy 2. Pathological labour 3. Medical diseases 4. Women who do not speak and undrestand danish

Design outcomes

Secondary

MeasureTime frame
use of oxytocinadditional need for oxytocin infusion in 1. stage and 2. stage
number of contractions/30 minutesnumber og contractions in 1st. stage and 2nd. stage

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026