Using dexmedetomidine for pain relief after cesarean sections

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of four different wound infiltration protocols on postoperative pain management in women undergoing cesarean sections. Participants will be randomly assigned to receive either dexmedetomidine, ropivacaine, a combination of both, or a placebo saline solution for pain relief at the surgical site. The study will measure pain intensity, morphine consumption, side effects, and overall satisfaction of the parturients. The goal is to determine the most effective method for reducing postoperative pain in this population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* pregnancy \>37 weeks, ASA I-II, BMI\<35

Exclusion Criteria:

* patient refusal, epilepsy, GERD, morbid obesity, drug allergy, ASA class \>2, presence of atrioventricular block, severe systemic disease, multiple gestation, high risk pregnancy, contraindications to epidural technique, a history of severe systemic disease, recreational drug or alcohol use

Where it's running

• Paraskevi K Matsota
  Athens, Other, Greece Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.