Skip to content

: Effect of warm shower and intravenous injection of hyoscine on the pain severity and duration of the active phase of labor in primiparous women

: Effect of warm shower and intravenous injection of hyoscine on the pain severity and duration of the active phase of labor in primiparous women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015012610324N22
Enrollment
162
Registered
2015-06-05
Start date
2015-04-21
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. Single spontaneous delivery

Interventions

Intervention 1: The control group will receive no intervention. Intervention 2: The first intervention group will receive hot shower for 20 minutes at 4 cm and 7 cm dilation. Intervention 3: The secon
Treatment - Other
Treatment - Drugs
The first intervention group will receive hot shower for 20 minutes at 4 cm and 7 cm dilation.
The second intervention group will receive Hyoscine at 4 cm and 7 cm dilation, 20 mg in ml intravenously diluted with 5 cc of distillated water.

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Being primiparous; Spontaneous starting of labor pain; Not suffering from disease; Normal fetal heart rate according to CTG; Cephalic presentation based on ultrasound; Desire to participate in study. Exclusion criteria: Having contraindication of normal delivery; Taking sedative and narcotic drugs during 48 hours prior to entering the study; Mental disorder history according to the patient's expression; Internal-surgical diseases including cardiovascular disease, thyroid disease, liver disease, kidney disease, asthma, epilepsy and etc according to the patient's expression; History of health problems in the current pregnancy according to the patient's expression; Participate in physiological childbirth classes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Labor pain severity. Timepoint: 30 minutes after the intervention. Method of measurement: Visual Analogue Scale.;Duration of active phase of labor. Timepoint: From 4 cm dilation to full dilation. Method of measurement: Partograph form in terms of minute.

Secondary

MeasureTime frame
Duration of second stage of labor. Timepoint: From full dilation until the newborn expulsion. Method of measurement: Partograph form in terms of minute.;Duration of third stage of labor. Timepoint: From newborn expulsion until placenta expulsion. Method of measurement: Partograph form in terms of minute.;Birth experience. Timepoint: 12 to 24 hours postpartum. Method of measurement: Birth experience scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mojgan Mirghafourvand

Tabriz University of Medical Sciences

Mirghafourvandm@tbzmed.ac.ir; Mirg1385@yahoo.com+98 41 3479 6770

Outcome results

None listed

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