CompletedNot Applicable

Propofol-ketamine or Propofol-fentanyl for Procedural Sedation in the Short-term Gynecological Case

Turkey (Türkiye)60 participantsStarted 2024-04-20

Plain-language summary

Comparison of fentanyl-propofol and ketamine-propofol combination for sedation in brief gynecological cases Our study aimed to evaluate ketamine-propofol and fentanyl-propofol combinations in short-term gynecological cases in terms of hemodynamic parameters, recovery, complications, patient and physician comfort.

Who can participate

Age range18 Years – 65 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: * Patients between the ages of 18-65, * American Society of Anesthesiologists (ASA) I-II, Exclusion Criteria: * Patients with a known allergy to any of the drugs used in the study, * Renal, hepatic, neuro-psychiatric, cardiovascular, or respiratory diseases, i * intracranial space-occupying lesions, * Pregnant women, * Body mass index (BMI) \> 30

What they're measuring

Surgical satisfaction

Timeframe: Postoperative procedure

Incidence of lower extremity movement during the procedure

Timeframe: intraoperative

Trial details

NCT IDNCT06412861

SponsorOndokuz Mayıs University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-06-30

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