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NCT ID: NCT02675634 Completed - Ileostomy Clinical Trials

Investigation of Two New 1-piece Ostomy Products in People With an Ileostomy or Colostomy

Start date: January 2016
Phase: N/A
Study type: Interventional

This clinical investigation is intended to explore the performance and safety of two newly developed ostomy products with regard to the products fit to body properties.

NCT ID: NCT02674919 Completed - Clinical trials for Repeated-sprint Ability

Nordic Hamstring and Repeated-sprint Ability in Football (Soccer) Players

Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate the efficacy of a 10-week intervention, using the Nordic Hamstring exercise, on repeated-sprint ability in male sub-elite football players. The primary outcome measure is total sprint time during 4x6 sprint of 10 meters measured using dual-beam photoelectric cells. Additionally, eccentric knee flexor strength is measured using the Nordbord hamstring strength measure. The hypothesis is that strength training of the knee flexor muscles elicited by the Nordic Hamstring exercise will result in enhanced repetitive sprint-ability expressed as a decrease in total sprint time. Furthermore, baseline data is used to assess to correlation between eccentric hamstring strength and active hamstring flexibility AND sprint performance.

NCT ID: NCT02674841 Completed - Clinical trials for Patellofemoral Pain Syndrome

Live Feedback to Increase Adherence in Adolescents With Patellofemoral Pain

Start date: February 2016
Phase: N/A
Study type: Interventional

This study investigates if live feedback during home-based exercises will improve the ability to perform the exercises with the prescribed time under tension (TUT) per repetition compared with no feedback among adolescents with patellofemoral pain. The hypothesis is that adolescents who receive live feedback from BandCizer™ will have a mean TUT that is significantly closer to the prescribed TUT compared to the group not receiving feedback during the course of the intervention.

NCT ID: NCT02674308 Completed - Clinical trials for Ulcerative Colitis and Crohn's Disease

Entyvio (Vedolizumab) Long Term Safety Study

Entyvio PASS
Start date: March 24, 2015
Phase:
Study type: Observational

The purpose of this study is to assess the long-term safety of vedolizumab versus other biologic agents in participants with Ulcerative Colitis (UC) or Crohn's Disease (CD).

NCT ID: NCT02673918 Completed - Breast Cancer Clinical Trials

The Breast Cancer Online Rehabilitation Program

BRECOR
Start date: February 2016
Phase: N/A
Study type: Interventional

The investigators have developed an online rehabilitation platform to guide women in their home-based upper-body exercises after breast cancer surgery. The platform includes rehabilitation videos that will guide the women in performing home-based early post-surgery upper-body rehabilitation tailored for each individual. The primary objective is to assess the feasibility and acceptability of a home-based rehabilitation program supported by a supplemental online platform for women after breast cancer surgery before conducting a larger pragmatic trial in the future. The feasibility of the platform will be tested in 11 municipalities in Denmark.

NCT ID: NCT02673801 Completed - Clinical trials for Osteoarthritis, Knee

Optimized Referral of Knee Patients to the Orthopedic Outpatient Clinic

Start date: August 2015
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate an algorithm to screen patients with suspected knee osteoarthritis referred to an orthopedic outpatient clinic by using radiographs and patient-reported symptoms. It will be investigated whether the algorithm is able to identify which patients that are deemed relevant to undergo an orthopedic assessment. This will be evaluated by estimating the sensitivity of the new algorithm compared to with the traditional clinical assessment of the patients.

NCT ID: NCT02673580 Completed - Epilepsy Clinical Trials

Tele-patient-reported Outcomes (telePRO) in Clinical Practice

Start date: January 2016
Phase: N/A
Study type: Interventional

The aim of this study is to compare quality of care and patient experiences in two outpatients follow-up activities: 1) Standard telePRO (fixed interval telePRO follow-up) and 2) Open Access telePRO (patient-initiated telePRO follow-up)

NCT ID: NCT02673164 Completed - Heart Failure Clinical Trials

Stem Cell Therapy in IschEmic Non-treatable Cardiac Disease

SCIENCE
Start date: January 2017
Phase: Phase 2
Study type: Interventional

The aim of the SCIENCE study is, in an international multicentre double-blind placebo-controlled study, to investigate efficacy of direct intra-myocardial injection of 100 mio. allogeneic Cardiology Stem Cell Centre_adipose derived stem cells (CSCC_ASCs) in patients with reduced left ventricular Ejection Fraction (EF) (≤45%) and heart failure.

NCT ID: NCT02673034 Completed - Infertility Clinical Trials

Circadian Variation in Serum-progesterone Levels Following Controlled Ovarian Hyperstimulation.

Start date: December 2014
Phase: N/A
Study type: Observational

The aim of the study is to investigate the circadian variation in serum-progesterone in women undergoing controlled ovarian stimulation.

NCT ID: NCT02672111 Completed - Opioid Use Disorder Clinical Trials

Long-Term Safety Study of Buprenorphine (CAM2038) in Adult Outpatients With Opioid Use Disorder

Start date: November 2015
Phase: Phase 3
Study type: Interventional

Open-label multi-center, 48 week safety study, consistent with standard practice for long-term safety studies. This one year safety study will utilize CAM2038 q1w (once weekly) and q4w (once monthly) and will have 3 phases: Screening, Treatment, and Follow-up.