Early Mobilisation Following Discectomy

NCT ID: NCT01710683

Last Updated: 2015-05-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

After lumbar discectomy 1st postoperative day high intensity exercise training reduced hospital stay, pain and sick leave without side effects in the two year follow-up period.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Postoperative pain is a major cause of delayed convalescence after discectomy. Different analgesic treatments with the use of local analgesics and steroid can reduce the immediate postoperative pain and convalescence after surgery. In orthopaedic and abdominal surgery accelerated stay programs with early mobilisation have reduced pain in the early postoperative periode. The late convalescence after discectomy for herniated disc disease can be reduced with the use of epidural steroids.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Reduced Hospital Stay Without Complication

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control group

Median age 45 years, 18-63.

Care program

Intervention Type BEHAVIORAL

Care program with multimodal pain treatment including epidural steroid

Intervention group

Median age 46 years, 18-62.

Care program

Intervention Type BEHAVIORAL

Care program with multimodal pain treatment including epidural steroid.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Care program

Care program with multimodal pain treatment including epidural steroid

Intervention Type BEHAVIORAL

Care program

Care program with multimodal pain treatment including epidural steroid.

Intervention Type BEHAVIORAL

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

No other names. No other names.

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with primary lumbar herniated disc disease who have received and performed a standardized conservative treatment program with intensive exercises.
* Oral and written acceptance.
* Age 18 and above.

Exclusion Criteria

* Patients with central or lateral spinal stenosis due to spondylosis or disc degeneration who needed bilateral decompression, laminectomy or fusion.
* Patients with cauda equina syndrome who needed acute operative treatment.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Vejle Hospital

OTHER

Sponsor Role collaborator

Copenhagen University Hospital, Denmark

OTHER

Sponsor Role collaborator

Northern Orthopaedic Division, Denmark

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Sten Rasmussen, M.D.

Role: PRINCIPAL_INVESTIGATOR

Northern Orthopaedic Department, Aalborg University Hospital, Denmark

David S. Krum-Moeller, M.D.

Role: STUDY_CHAIR

Department of Orthopaedic Surgery, Vejle and Give Hospital

Lene R. Lauridsen, M.D.

Role: STUDY_CHAIR

Department of Orthopaedic Surgery, Vejle and Give Hospital

Henrik Kehlet, M.D.

Role: STUDY_CHAIR

Section for Surgical Pathophysiology, Juliane Marie Centre, Rigshospitalet, Copenhagen

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Northern Orthopaedic Division, Aalborg Hospital, Aarhus University

Aalborg, , Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ON-07-006

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Running Related Injury Among Novice Runners
NCT02014987 UNKNOWN EARLY_PHASE1
Assessing the Acute Effects of Diagonal Mobilization
NCT06719752 ENROLLING_BY_INVITATION NA
Lyske Trial (Danish) Groin Trial
NCT00226603 UNKNOWN PHASE2/PHASE3