Fusion of Spine, Lumbar Region

2

Review clinical trials related to Fusion of Spine, Lumbar Region. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effects of Erector Spinae Plane Block on Postoperative Pain Following Lumbar Fusion Surgery

The purpose of this study is to determine if the method for injecting local anesthesia affects patients' pain and opioid usage after surgery. The investigators will compare subcutaneous anesthesia, injections of anesthesia under the skin, to a method called erector spinae plane block (ESPB). An ESPB injection involves placing local anesthesia along the muscles and bones in the back, using a special type of x-ray called fluoroscopy for guidance. The Investigators will use patient reported outcomes (PROs) and track subjects' opioid usage to find out if there is a difference between ESPB and subcutaneous anesthesia. The investigators hypothesize that patients who get ESPB injections will use less opioids and report less pain after lumbar fusion surgery compared to patients who receive subcutaneous anesthesia injections.

Participants needed: 66
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Massachusetts, WorcesterUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

The individual has signed and dated a study specific informed consent form appro... [+3]

Patients unable to consent for themselves. [+6]

Status: Recruiting

Echo-guided Transverse Abdominal Plane Block (TAP) in Anterior Lumbar Arthrodesis (ALIF)

The goal of this interventional study is to is to compare the effect of a tap block versus a placebo in patients undergoing anterior lumbar spine surgery. The main question it aims to answer : • whether tap block can reduce the need for postoperative pain medication Participants will be randomized into two groups and all postoperative pain medication will be recorded over 3 days. Researchers will compare tap block vs placebo to see if it reduces postoperative pain.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Clinique Saint Jean, FranceUpdated: Jan 6, 2026Locations: 1
Eligibility criteria

Patient who has been informed about the study and has co-signed a consent form w... [+2]

Patients with intolerance or contraindication to paracetamol, anti-inflammatory... [+9]