Pain relief in laour with remifentanil and ketamine
Phase 2
- Conditions
- pain relief during labour.Spontaneous vertex delivery
- Registration Number
- IRCT201108241952N3
- Lead Sponsor
- Arash Women's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
nulliparous, ASA I, II, gestational age 38-42 weeks in early labour
Exclusion criteria: weight less than 50 kg more than 100 kg, candidate to undergo epidural analgesia, multifetus pregnancy, pre-eclampsia, premature labour, allergy to any agent under investigation, history of alcohol or drug abuse, psychiatric disorder
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain relief during labor. Timepoint: from active labor phase (cervical dilation 4-5 cm) until labour. Method of measurement: VAS score.
- Secondary Outcome Measures
Name Time Method Heart rate. Timepoint: every 30 minutes. Method of measurement: pulse-oximetry.;SPO2. Timepoint: every 30 minutes. Method of measurement: pulse-oximetry.;Respiratory rate. Timepoint: every 30 minutes. Method of measurement: visual monitoring.;Fetal heart rate. Timepoint: every 30 minutes. Method of measurement: surface ultrasound.;Present or absent of nausea and vomiting. Timepoint: every time is peresent. Method of measurement: visual monitoring and patient's saying.;Overall effective analgesia. Timepoint: every 30 minutes after statring analgesia. Method of measurement: VAS score.;Arterial pressure. Timepoint: every 30 minutes after statrting analgesia. Method of measurement: non-invasive arterial presssure monitoring.