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NCT06849661
Do Preoperative Bilirubin Levels Affect Recovery and Hospital Stay After Sedation Anesthesia?
trial in Preoperative Biliary Drainage in 360 participants. Enrolling by invitation.
15 September 2025
Quick facts
| Lead sponsor | Naime Yalçın |
|---|---|
| Status | ENROLLING BY INVITATION |
| Study type | OBSERVATIONAL |
| Enrollment | 360 |
| Start date | 15 January 2025 |
| Primary completion | 15 September 2025 |
| Estimated completion | 1 October 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- Preoperative Biliary Drainage — all drugs for Preoperative Biliary Drainage →
- Recovery Period, Anesthesia — all drugs for Recovery Period, Anesthesia →
- Hospital Length of Stay — all drugs for Hospital Length of Stay →
Sponsor
Naime Yalçın
Who can join
18 and older, any sex, with Preoperative Biliary Drainage or Recovery Period, Anesthesia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
There are still complexities regarding the effects of anesthetic drugs on bilirubin metabolism. The aim of the study was to investigate whether preoperative serum bilirubin levels are associated with the length of hospital stay after ERCP performed under sedation anesthesia in the presence of propofol. Unstable hemodynamics, increased propofol sensitivity, and prolonged recovery time to anesthetics are common features encountered in patients with hyperbilirubinemia. Therefore, close monitoring of cardiovascular functions in these patients and awareness of the possible need for a reduction in the dose of anesthetic used are the expected benefits of the study.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
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Related trials
Other Naime Yalçın trials
Trials by the same sponsor.
- NCT06824935 — Evaluation of Perioperative Anesthesia Requirements of Outpatient Cataract Patients · enrolling by invitation
- NCT06810232 — Effects of General Health Risk Factors on Prolonged Hospital Stay · enrolling by invitation
- NCT06865378 — The Correlation Between Intraoperative End Tidal Carbon Dioxide, Perfusion Index and Pulse Variability Index on Postoper · enrolling by invitation
- NCT06843031 — The Role of Perfusion Index in Defining Postoperative Shivering · active not recruiting
- NCT06837415 — Association Between Preoperative Anxiety and Blood Eosinophil Levels · enrolling by invitation
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06849661 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Naime Yalçın
- Last refreshed: 27 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06849661.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing