Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02855567 · ClinicalTrials.gov registry record · NA
Acupuncture for Post-Operative Pain Control for Patients Undergoing Gynecological Surgery
A NA study of Postoperative Pain and Acupuncture, sponsored by Icahn School of Medicine at Mount Sinai.
- Completed
- Registry status
- NA
- Development phase
- 110
- Enrollment target
- 1
- Study location
NCT02855567: Completed NA study of Postoperative Pain and Acupuncture, sponsored by Icahn School of Medicine at Mount Sinai.
NCT02855567 is a NA study of Postoperative Pain and Acupuncture that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 110 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02855567, a NA study of Postoperative Pain and Acupuncture, has completed, sponsored by Icahn School of Medicine at Mount Sinai.
- COMPLETED
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
- 1
- Study location
Study Summary
This study investigates the role of acupuncture in controlling post-operative pain in patients who have undergone gynecological surgery.
Primary Outcome
Effectiveness of intra-operative acupuncture in post-operative pain control as measured by narcotic use in the 24 hours post-operatively. Narcotic use monitored either through hospital records if patient is still admitted to the hospital or over the phone if the patient is discharged home prior to 24 hours post-operative.
Conditions Studied
Interventions
- DEVICE Acupuncture needles
Study Locations (1)
New York
- Icahn School of Medicine at Mount Sinai - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2016-08-06 |
| Est. Completion | 2017-12-05 |
| Phase | NA |
What the finished NCT02855567 record still lists
NCT02855567 is an interventional study that assigns participants to a tested intervention. The registered 110 participants enrollment target is mid-sized for trials with a published cap, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (52% lower).
The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which Acupuncture needles is the first listed.
NCT02855567 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT02855567 about?
NCT02855567 is a clinical study titled "Acupuncture for Post-Operative Pain Control for Patients Undergoing Gynecological Surgery". This study investigates the role of acupuncture in controlling post-operative pain in patients who have undergone gynecological surgery.
What is the current status of trial NCT02855567?
This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2016-08-06. Estimated completion is 2017-12-05.
What conditions does trial NCT02855567 study?
This clinical trial studies the following conditions: Postoperative Pain, Acupuncture, Gynecological Surgery.
What interventions are being tested in trial NCT02855567?
The interventions under investigation include: Acupuncture needles (DEVICE).
Who is sponsoring clinical trial NCT02855567?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02855567 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 Pain
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 NCT02855567's enrollment target sits among peer trials
110 52nd of 120 higher than 69 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain 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
-
Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery
RECRUITING · NA
-
Virtual Reality and Olfactory Stimuli Multimodal Intervention to Reduce Post-Operative Pain and Anxiety in Patients Undergoing Cardiothoracic Surgery
RECRUITING · NA
-
Rectus Sheath Block in Cardiac Surgery
RECRUITING · NA
-
Pain With Differing Insufflation Pressures During Laparoscopic Hysterectomy
RECRUITING · NA
-
Effects of Assisted Robotic vs Laparoscopic Sleeve Gastrectomy
RECRUITING · NA
-
Postoperative Pain Control in AIS Using Liposomal Bupivacaine vs. 0.25% Bupivacaine With Epinephrine
RECRUITING · NA
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
- NCT01530373 · 110 participants · Phase 2
Solifenacin Compared to Clonidine for Reducing Hot Flashes Among Breast Cancer Patients
- NCT02379377 · 110 participants · Phase 1
18F-FSPG PET in Imaging Patients With Liver Cancer Before Undergoing Surgery or Transplant
- NCT02411773 · 110 participants · Phase 1
Sympatholysis in Chronic Kidney Disease
- NCT03190941 · 110 participants · Phase 1
Administering Peripheral Blood Lymphocytes Transduced With a Murine T-Cell Receptor Recognizing the G12V Variant of Mutated RAS in HLA-A*11:01 Patients
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI