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NCT ID: NCT04204720 Completed - Clinical trials for Spinal Stenosis Lumbar

A Comparison of Intravascular Injection With Chiba Needle and Whitacre Needle

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Caudal epidural injection (CEI) is effective for spinal pain. However, intravascular injection may occur during CEI, which can lead to hematoma, neurologic deficit and local anesthetics systemic toxicity. Whitacre type needle has been reported to be effective for reducing intravascular injection during transforaminal epidural injection. In this study, we compared the Chiba needle and Whitacre needle on incidence of intravascular injection during CEI.

NCT ID: NCT04236193 Completed - Clinical trials for Shoulder Injury Related to Vaccine Administration

Ultrasound and Immunological Findings in Patients With Shoulder Injury Related to Vaccine Administration (SIRVA)

SIRVA
Start date: April 1, 2018
Phase:
Study type: Observational [Patient Registry]

Accidental vaccine injection into adjunct shoulder structures can cause tissue damage, termed Shoulder injury related to vaccine administration (SIRVA). The immunopathological mechanisms and consequences of SIRVA are unknown. The study assesses the clinical and immunological consequences of an influenza vaccine if accidentally administered in periarticular space.

NCT ID: NCT04251598 Completed - Health Behavior Clinical Trials

I am Protecting my Child From the Sun Program

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to examine the effect of the "I Am Protecting My Child from the Sun" program, based on social cognitive theory, on parents' sun-protection product use and sun avoidance behaviors. The "I Am Protecting My Child from the Sun" program, based on Social Cognitive Theory, and the sending of short reminder messages had positive effects on the parents' behaviors related to protecting themselves and their children from the sun.

NCT ID: NCT04254601 Completed - Skin Diseases Clinical Trials

Laser Therapy Versus Narrow Band Ultraviolet B for the Treatment of Acne Vulgaris

LLLT-NBUB
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Forty-five participants with facial AV were assigned randomly to three groups of fifteen subjects each. Each group received various therapies. Group A (Study group A) had received both NBUB and akne-Mycin; Group B( study group B) had received Red LLLT and akne-Mycin and group C (Control group) received only akne-Mycin cream. All 45 participants are tested at the initial treatments, after 4 weeks and after 8 weeks by the acne count, the intensity scale and the photographic test.

NCT ID: NCT04257539 Completed - Clinical trials for Chronic Low-back Pain

Reducing Sedentary Time in Chronic Low Back Pain: Sedentary Intervention Using Motivational Interviewing and Technology

SUMIT
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

This study will test the effects of a sedentary behavior intervention on pain processing, blood bio-markers and pain symptoms in individuals with chronic low back pain. The behavioral intervention will include a wrist-worn activity monitor that will notify participants when they have been sedentary for too long, motivational interviewing, and habit development.

NCT ID: NCT04267991 Completed - Corneal Disease Clinical Trials

Corneal Densitometry Changes With Adenoviral SEI

Start date: April 1, 2018
Phase:
Study type: Observational

Adenoviral Sub epithelial infiltrates (SEI) affect ocular function.They lead to reduced vision, photophobia, glare, halos, and foreign body sensation.

NCT ID: NCT04268082 Completed - Clinical trials for Total Hip Replacement

Insole-based Visual Biofeedback for Weight-bearing in Total Hip Replacement

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The study investigates the effects of visual biofeedback, based on a sensorized system for the dynamic evaluation of the plantar pressure versus rehabilitation with traditional verbal instructions of the physiotherapist, on weight bearing distribution in patients who underwent first total hip replacement. The study is a randomized controlled trial, with parallel groups, without blinding.

NCT ID: NCT04294732 Completed - Clinical trials for Peripheral Nerve Block

Efficacy of Popliteal Block and Bupivacaine Concentration Used for Analgesia in Foot and Ankle Surgery

Start date: April 1, 2018
Phase: Phase 4
Study type: Interventional

In the orthopedic foot and ankle surgeries, the effects of postoperative popliteal nerve block applied for palliation of pain and local anesthetic agent in two different concentrations (0.166 and 0.250) which were used in popliteal nerve block procedure, will be investigated.

NCT ID: NCT04301037 Completed - Clinical trials for Medial Malleolus Fracture

Tension Band Wiring Versus Cannulated Screws in Fixation of Medial Malleolus in Ankle Fracture

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

This is a prospective randomized study conducted on 30 patients with an age spanning between 20 and 55 years. Half of the sample was treated by tension band wiring for closed medial malleolar fractures, and the other half by two cannulated screws. The patients were assessed at (6w-3months and 6months) for clinical and radiological union and evaluated functionally (12 months) using modified Olerund and Molander scoring system.

NCT ID: NCT04304404 Completed - Breast Cancer Clinical Trials

Risk Reduction Program for Women Having High Risk of Breast Cancer

BrCaRRP
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

An intervention program involving education, guidance, counseling, case management and surveillance based on the Health Belief Model will be implemented on women with high risk of breast cancer. The impact of the breast cancer risk reduction program on participation in breast cancer screenings, health beliefs (health motivation, sensitivity, fear of breast cancer) and behaviors (physical activity, nutrition, health responsibility, genetic counseling) will be evaluated in the study.