Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Peri-Operative Testosterone Administration in Primary Total Hip Arthroplasty

It is often observed that patients following total hip replacement have a hard time with rehabilitation, as patients commonly lose muscle mass and strength around the surgical site. The goal of this study is to learn if giving patients testosterone around their hip surgery can prevent them from losing muscle mass, as well as to see if it will improve their outcomes after surgery. The main question this study aims to answer is: Will perioperative testosterone administration increase lean mass in addition to improving functional and clinical patient reported outcomes greater than placebo? Researchers will compare patients who were administered testosterone to standard of care (no administration of testosterone) to see if there is a difference in their recovery and outcomes. Participants will be given either testosterone or saline for eight weeks beginning two weeks prior to surgery. Participants will have to answer questionnaires on how they are doing, as well as will do other testing during this time.

Participants needed: 60
Trial details
Phase: Phase 4Age: 18+Biological sex: MaleType: InterventionalSponsor: American Hip InstituteUpdated: Jan 1, 2025
Eligibility criteria

Male patients over the age of 18 with a diagnosis of osteoarthritis or dysplasia...

Major exclusion criteria include previous arthroplasty of the affected hip, prev...

Status: Not yet recruiting

Peri-Operative Testosterone Administration in Primary Hip Arthroscopy

It is often observed that patients following hip surgery have a hard time with rehabilitation, as patients commonly lose muscle mass and strength around the surgical site. The goal of this study is to learn if giving patients testosterone around their hip surgery can prevent them from losing muscle mass, as well as to see if it will improve their outcomes after surgery. The main question this study aims to answer is: Will perioperative testosterone administration increase lean mass in addition to improving functional and clinical patient reported outcomes greater than placebo? Researchers will compare patients who were administered testosterone to standard of care (no administration of testosterone) to see if there is a difference in their recovery and outcomes. Participants will be given either testosterone or saline for eight weeks beginning two weeks prior to surgery. Participants will have to answer questionnaires on how they are doing, as well as will do other testing during this time.

Participants needed: 60
Trial details
Phase: Phase 4Age: 18-90Biological sex: MaleType: InterventionalSponsor: American Hip InstituteUpdated: Jan 1, 2025
Eligibility criteria

Male patients over the age of 18 with a diagnosis of femoroacetabular impingemen...

. Major exclusion criteria include previous surgery to the affected hip or spine...

Status: Recruiting

Knotless Implants As an Alternative for Capsular Closure in Primary Hip Arthroscopy: a Prospective, Multi-Center Study

The purpose of this research is to see if the Arthrex LoopLocTM device is better for capsular closure during hip arthroscopy than other treatments available. The hip capsule is the tissue that surrounds your hip joint. It stabilizes and supports your hip joint. During hip arthroscopy, this tissue must be cut through in order to perform the hip arthroscopy. Once the hip arthroscopy is completed, the surgeon might repair the capsule. Current ways of repairing the capsule include knotted suture that might irritate structures around the hip, leading to the possible formation of scar tissue and pain. The Arthrex LoopLocTM device is knotless and may lower the presence of irritation and scar tissue around the hip after surgery and might lead to better outcomes. Therefore, researchers will compare patients who had the LoopLocTM device used to close their hip capsule during surgery to those who did not have the device used, to see if there is a difference in their outcomes following surgery.

Participants needed: 80
Trial details
Phase: Phase 4Age: 18-60Biological sex: AllType: InterventionalSponsor: American Hip InstituteUpdated: Jan 1, 2025Locations: 1
Eligibility criteria

Patients undergoing a primary hip arthroscopy [+2]

Patients that had previous hip surgery, [+2]

Status: Not yet recruiting

Intraoperative Bone Marrow Aspirate Concentrate Injections: Evaluating Outcomes in a Randomized Controlled Trial

The purpose of this study is to see if bone marrow aspirate concentrate (BMAC) used with your hip arthroscopy surgery is a better treatment than just having surgery alone for treatment of labral tears in your hip. BMAC is an injection, where your doctor will insert a needle into your hip and harvest the bone marrow that is located inside of your bones. This will be performed under anesthesia during your hip arthroscopy surgery and will be injected during the procedure. BMAC is an FDA approved procedure and has had many research articles produced from it. Researchers will compare patients who received BMAC during their surgery to those who have not to determine if the injection with surgery is better than surgery alone.

Participants needed: 80
Trial details
Phase: Phase 4Age: 16+Biological sex: AllType: InterventionalSponsor: American Hip InstituteUpdated: Dec 27, 2024
Eligibility criteria

Patients undergoing primary hip arthroscopy to treat femoroacetabular impingemen... [+2]

Patients who have had prior hip arthroscopy or hip surgery, Tonnis grade II or h... [+1]