Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01880164 · ClinicalTrials.gov registry record

Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity

A clinical trial of Spinal Deformity, sponsored by Shay Bess.

Completed
Registry status
21
Enrollment target
10
Study locations

NCT01880164: Completed study of Spinal Deformity, sponsored by Shay Bess.

NCT01880164 is a study of Spinal Deformity that has completed, run by Shay Bess. The registered enrollment target is 21 participants, below the 620-participant average among 7 other Spinal Deformity trials with a reported enrollment target (97% lower). The trial reports 10 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01880164, a study of Spinal Deformity, has completed, sponsored by Shay Bess.

COMPLETED
Registry status
21 participants
Enrollment target
10
Study locations

Study Summary

Quantify the efficacy and cost of nonoperative treatment modalities used for adult spinal deformity.

Primary Outcome

This questionnaire has been designed to provide information as to how back pain affects ability to manage in everyday life. Score must be equal to or greater than 30 for eligibility to enroll.

Conditions Studied

Study Locations (10)

California

  • University of California - Davis - Sacramento
  • University of California - San Francisco Medical Center - San Francisco

New York

  • NYU Hospital for Joint Diseases - New York
  • Hospital for Special Surgery - New York

Colorado

  • Rocky Mountain Scoliosis and Spine - Denver

Kansas

  • University of Kansas Medical Center - Kansas City

Kentucky

  • Norton Leatherman Spine Center - Louisville

Missouri

  • Washington University at St. Louis - St Louis

Oregon

  • Oregon Health Sciences University - Portland

Virginia

  • University of Virginia - Charlottesville

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2015-06
Est. Completion 2017-04
Shay Bess

2 total trials

What the finished NCT01880164 record still lists

NCT01880164 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 620-participant average among 7 other Spinal Deformity trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Spinal Deformity appearing as the primary indexed condition, and to 0 interventions.

NCT01880164 lists 10 locations in 8 states (California, New York, Colorado).

Frequently Asked Questions

What is clinical trial NCT01880164 about?

NCT01880164 is a clinical study titled "Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity". Quantify the efficacy and cost of nonoperative treatment modalities used for adult spinal deformity.

What is the current status of trial NCT01880164?

This trial is currently completed. The enrollment target is 21 participants. The study started on 2015-06. Estimated completion is 2017-04.

What conditions does trial NCT01880164 study?

This clinical trial studies the following conditions: Spinal Deformity.

Who is sponsoring clinical trial NCT01880164?

This trial is sponsored by Shay Bess, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01880164 being conducted?

This trial has 10 study locations across California, Colorado, Kansas, Kentucky, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Spinal Deformity

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.

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

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer

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

Source: ClinicalTrials.gov NCT01880164, the US trial registry maintained by the National Library of Medicine. NCT01880164 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.