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Rupture clinical trials

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NCT ID: NCT06114368 Enrolling by invitation - Clinical trials for Achilles Tendon Rupture

Endoscopic Flexor Hallucis Longus Transfer vs Minimally Invasive Repair in Acute Achilles Tendon Rupture

Start date: March 5, 2023
Phase:
Study type: Observational

The goal of this observational study is to compare the outcomes of two different surgical techniques (Endoscopic Flexor Hallucis Longus transfer - Group 1 vs Minimally Invasive primary repair - Group 2) for patients with acute Achilles tendon rupture. The main questions to be answered are: 1. Which group's patients are more satisfied? 2. Which group's patients appear to have a greater complication rate? 3. Which group's patients have greater calf and ankle circumference compared to the unaffected limb? 4. Which group's patients have greater passive and active range of ankle motion compared to the unaffected limb? 5. Are group 1 patients characterized by strength deficit in hallux flexion power?

NCT ID: NCT05912634 Enrolling by invitation - Aortic Dissection Clinical Trials

Repair Versus Non-repair of the Aortic Arch in Type A Aortic Dissection (TAAD)

AoArch
Start date: January 30, 2022
Phase:
Study type: Observational

Acute Stanford type A aortic dissection (TAAD) is a life-threatening clinical status requiring surgery that is usually performed as a salvage procedure.We planned a multicenter study to evaluate the balance between the patient's condition and those therapeutic strategies that may limit the risk of late adverse events in patients who will be underwent surgery for appropriate management of TAAD

NCT ID: NCT05763069 Enrolling by invitation - Preeclampsia Clinical Trials

HOME: Home Monitoring of High-risk Pregnancies

Start date: November 21, 2022
Phase:
Study type: Observational [Patient Registry]

High-risk pregnancies often require long-term hospitalization or outpatient maternal and/or fetal monitoring, placing a burden on patients, hospital resources and society. The demand for intensified pregnancy surveillance and interventions is increasing, due to the increased prevalence of risk factors like obesity and advanced maternal age, as well as altered guidelines resulting in increasing labor induction rates.The main aims of the HOME study (Home monitoring of pregnancies at risk) are to assess if home monitoring of selected high-risk pregnancies for maternal and fetal wellbeing is feasible, safe (in a clinical trial), cost-efficient, and simultaneously empowers the users.

NCT ID: NCT05614908 Enrolling by invitation - Clinical trials for Achilles Tendon Rupture

Outcome After Conservatively Treated Achilles Tendon Rupture

Start date: November 1, 2022
Phase:
Study type: Observational

The main purpose of the study is to investigate self-reported functional ability of patients undergoing conservatively treated achilles tendon rupture at 6, 12 and 24 months from the date of injury.

NCT ID: NCT04650568 Enrolling by invitation - Clinical trials for Anterior Cruciate Ligament Rupture

Biologic Augmentation With Mesenchymal Stem Cells in Patients Undergoing Anterior Cruciate Ligament Reconstruction

BMAC
Start date: November 3, 2017
Phase: N/A
Study type: Interventional

This study will evaluate the efficacy of biologic augmentation of ACL reconstruction with bone marrow derived mesenchymal stem cells as measured by magnetic resonance imaging to detect graft healing and integration. Secondary endpoints will include validated patient reported outcome measures, as well as functional outcome using objective examination findings.

NCT ID: NCT04451109 Enrolling by invitation - Clinical trials for Gestational Diabetes

Dilapan-S®: A Multicenter US E-registry

Start date: December 1, 2020
Phase:
Study type: Observational

Objective of this registry is to collect a representative set of real world data on the use of Dilapan-S® for pre-induction cervical ripening in daily clinical practice. Upon completion of the registry, relevant collected data will be analyzed and published.

NCT ID: NCT04269447 Enrolling by invitation - Aortic Aneurysm Clinical Trials

Prospective Aortic Biobank of POP-STAR

Start date: November 18, 2019
Phase:
Study type: Observational [Patient Registry]

The overall objective of the POP-STAR project is individualized surveillance for patients diagnosed with abdominal aortic aneurysms by means of more precise, patient-specific AAA growth prediction.

NCT ID: NCT03365908 Enrolling by invitation - Clinical trials for Anterior Cruciate Ligament Rupture

Pain Management of ACL Reconstruction

Start date: October 9, 2017
Phase: N/A
Study type: Interventional

This study will compare the outcome of pain interventions that are considered standard of care during the surgical treatment of ACL injuries. The comparison will be looking at pain control during and after ACL surgery as well as functional outcomes in patients that had a nerve block versus those who did not. The investigators hypothesize that pain control will be equal between both groups.

NCT ID: NCT02469792 Enrolling by invitation - Clinical trials for Anterior Cruciate Ligament Partial Rupture

Effectiveness and Safety of Autologous ADRC for Treatment of Anterior Cruciate Ligament Partial Rupture

Start date: June 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Autologous adipose-derived regenerative cells (ADRC) will be extracted using Celution 800/CRS System (Cytori Therapeutics Inc) from a portion of the fat harvested from the patient's front abdominal wall. Patients will undergo knee arthroscopic surgery followed by one-time intraarticular ADRC administration (directly into anterior cruciate ligament). This is a single arm study with no control. All patients receive cell therapy.