Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02325154 · ClinicalTrials.gov registry record · NA
Cerebral Oxygenation in Total Hip Arthroplasty Patients
A NA study of Postoperative Delirium and Cerebral Oxygen Desaturation, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT02325154: Completed NA study of Postoperative Delirium and Cerebral Oxygen Desaturation, sponsored by Hospital for Special Surgery, New York.
NCT02325154 is a NA study of Postoperative Delirium and Cerebral Oxygen Desaturation that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 100 participants, below the 170-participant average among 8 other Postoperative Delirium trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02325154, a NA study of Postoperative Delirium and Cerebral Oxygen Desaturation, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
We plan to investigate the relationship between hypotensive epidural anesthesia for hip arthroplasty and cerebral oxygen saturation.
Primary Outcome
The number of participant's experiencing an intra-operative cerebral oxygen desaturation event. Measured in the number of patients, beginning with the time the patients' enters the operating room and up to 4 hours.
Conditions Studied
Interventions
- DEVICE Cerebral Oximeter
Study Locations (1)
New York
- Hospital for Special Surgery - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2014-12 |
| Est. Completion | 2016-08 |
| Phase | NA |
What the finished NCT02325154 record still lists
NCT02325154 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 170-participant average among 8 other Postoperative Delirium trials with a reported enrollment target (41% lower).
The record links to 2 conditions, with Postoperative Delirium appearing as the primary indexed condition, and to 1 intervention - of which Cerebral Oximeter is the first listed.
NCT02325154 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT02325154 about?
NCT02325154 is a clinical study titled "Cerebral Oxygenation in Total Hip Arthroplasty Patients". We plan to investigate the relationship between hypotensive epidural anesthesia for hip arthroplasty and cerebral oxygen saturation.
What is the current status of trial NCT02325154?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2014-12. Estimated completion is 2016-08.
What conditions does trial NCT02325154 study?
This clinical trial studies the following conditions: Postoperative Delirium, Cerebral Oxygen Desaturation.
What interventions are being tested in trial NCT02325154?
The interventions under investigation include: Cerebral Oximeter (DEVICE).
Who is sponsoring clinical trial NCT02325154?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02325154 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Delirium
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02325154's enrollment target sits among peer trials
100 5th of 8 higher than 3 of 8 other Postoperative Delirium trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Delirium trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Digital Sleep Optimization for Brain Health Outcomes in Older Surgical Patients
RECRUITING · NA
-
A Clinical Trial of Intravenous Lidocaine After Spinal Surgery to Prevent Delirium and Reduce Pain
RECRUITING · Phase 3
-
CEReBral AutorEgulation in Non-cardiac SuRgery and Relationship to Postoperative DeliriUm State
RECRUITING
-
The Caffeine, Postoperative Delirium, and Change in Outcomes After Surgery (CAPACHINOS-2) Study
RECRUITING · Phase 2
-
Efficacy of Suvorexant on Post-operative Sleep Disturbance
RECRUITING · Phase 4
-
Daridorexant to Prevent Post-cardiotomy Delirium
RECRUITING · Phase 2
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01048281 · 100 participants
Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma
- NCT01161199 · 100 participants
The Use of Leukapheresis to Support HIV Pathogenesis Studies
- NCT01327690 · 100 participants · Early Phase 1
Mental Health in Veterans and Families After Group Therapies
- NCT01730781 · 100 participants
Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia