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delivery

Comparison of effects of transcutaneous electrical nerve stimulation and of pharmaceutical hyoscine– promethazine compound on duration of the second phase of labor

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201604144317N10
Enrollment
84
Registered
2017-03-14
Start date
2015-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

delivery. Pregnancy, childbirth and the puerperium

Interventions

Intervention 1: At the onset of active labor phase (4-cm dilatation), medication group subject were injected once intramuscularly by 20 mg of hyoscine and 25 mg of promethazine simultaneously. Interve
Treatment - Drugs
At the onset of active labor phase (4-cm dilatation), medication group subject were injected once intramuscularly by 20 mg of hyoscine and 25 mg of promethazine simultaneously.
For TENS group, was used with 1 pair of upper electrodes placed between L1-T10 and 1 pair of lower electrodes placed between S2-S4 apart 7 cm from both side of spinal column. Tens being on/off for 20

Sponsors

shahid beheshti university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Being of Iranian race; 2. The first and /or the second labor; 3. Being 18-35 years of old; 4. Term pregnancy, single-twin, and presentation of fetus head; 5. Onset of spontaneous contractions; 6. Dilatation examination upon arrival at 3-4 cm; 7. Minimum education level of elementary grade 5; 8. Not taking painkillers 3 hours before and during study; 9. Mot more than 6 hours passed after caul rupture; 10. Lack of experience with TENS; 11. No epilepsy; 12. No cardiac pacemakers; 13. No use of substance/ drugs; and 14. No skin lesions or surgical scars at the place of electrodes. And followings are criteria for women ti be excluded from the study; 1. Emergency caesarean prior to the study completion; research; 2. Occurrence of such labor complications as vaginal bleeding during research; 3. Patients reluctance to continue participating in the study; and 4. Wounds or scars present at the place of electrodes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: At 4-5 cm, 6-7 cm, 8-9cm, 10cm. Method of measurement: pain visual scale.

Secondary

MeasureTime frame
Duration of the first phase of labor. Timepoint: duration of the first phase((upon arrived until 10-cm dilatation). Method of measurement: wristwatch.;Duration of the second phase of labor. Timepoint: second phase (from 10-cm dilatation to the fetus exit). Method of measurement: wristwatch.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactfateme nahidi

shahid beheshti university of medical sciences

nahidi@sbmu.ac.ir+218 8202512

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026