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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02135224
Other study ID # M79
Secondary ID
Status Recruiting
Phase N/A
First received May 6, 2014
Last updated May 7, 2014
Start date December 2011

Study information

Verified date May 2014
Source University of Athens
Contact Chryssoula V Staikou, PhD
Phone 00302107286000
Email c_staikou@yahoo.gr
Is FDA regulated No
Health authority Greece: Ethics Committee
Study type Interventional

Clinical Trial Summary

The study hypothesis was that epidural fentanyl may accelerate the dilation of the cervix and possibly result in a shorter duration of vaginal delivery.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- American Society of Anaesthesiologists physical status I or II

- nulliparous

- normal singleton uncomplicated pregnancies of more than 38 weeks

- cephalic presentation of the fetus

- anticipated vaginal delivery

- active stage of labour

- cervical dilatation between 3-5 cm

- regular uterine contractions

- normal cardiotocographic recordings.

Exclusion Criteria:

- medical problems during pregnancy

- BMI=40 kg m-2

- opioid allergy

- prior administration of opioids or other analgesics

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
Fentanyl

Normal saline


Locations

Country Name City State
Greece Aretaieio Hospital, University of Athens Athens Attiki

Sponsors (1)

Lead Sponsor Collaborator
University of Athens

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Other duration of delivery min between first epidural dose and delivery of the baby No
Primary cervical dilatation every 60 min starting from the first epidural dose up to cervical dilatation of 10 cm No
Secondary Bishop score based on Cervical Position, Effacement, Dilation, Softness and Fetal Station. Bishop score is a pre-labor scoring system which reflects the stage of the procedure (mainly the cervix condition) assessing the following: Cervical Position, Effacement, Dilation, Softness and also Fetal Station. every 60 min from the time the first epidural dose is administered up to delivery No
See also
  Status Clinical Trial Phase
Recruiting NCT06053073 - Induction to Labour With Double Cervical Ballon at Home Versus at Hospital N/A