Not Yet RecruitingPhase 1

Spinal Analgesia in Labour Pain

Egypt100 participantsStarted 2025-12-24

Plain-language summary

To evaluate the efficacy and safety of dexmedetomidine as an adjuvant to bupivacain and fentanyl in spinal Analgesia to decreases pain during normal labour

Who can participate

Age range18 Years – 40 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Age of patint is between 18 and 40 years. gestational age of fetus is more than 37 weeks. singleton viable fetus and cephalic presentation. spontaneous labor with cervix dilation more than 5cm. Exclusion Criteria: Drug allergy. Blood Disease. Infection at site of injection. patient takes anticoagulants. patient has pre-eclampsia ,cardiac disease (NYHA III-IV) or diabetes mellitus type I prior to the pregnancy patients refuse

What they're measuring

changes in numeric pain intensity score ( NPSI) maximum 10 minimum 0

Timeframe: baseline

duration of sensory blockade

Timeframe: 5 minutes after injection of analgesic agents till normal delivery done

changes in numeric pain intensity score ( NPIS )

Timeframe: 5 minutes, 10 minutes, 15 minutes, 30 minutes and 45 minintes after injection of analgesic agents

Trial details

NCT IDNCT07332130

SponsorMinia University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-01-10

Contact for this trial

Mohamed Ragab, Master

086-01001737436 mohamedragab2209@gmail.com

View on ClinicalTrials.gov More Labour Analgesia trials