Clinical Trials Logo

Other clinical trials

View clinical trials related to Other.

Filter by:

NCT ID: NCT03510416 Not yet recruiting - Clinical trials for Hepatocellular Carcinoma Refractory to Transcatheter Arterial Chemoembolization

Efficacy and Safety of Apatinib Combined With TACE in Patients With Hepatocellular Carcinoma

Start date: May 1, 2018
Phase: Phase 2
Study type: Interventional

Efficacy and Safety of Apatinib Combined With TACE in Patients With Hepatocellular Carcinoma Refractory to Transcatheter Arterial Chemoembolization .

NCT ID: NCT03507153 Not yet recruiting - Clinical trials for Maxillary Class III Modification I Edentulous Patients

Muscle Activity Evaluation of Maxillary Bilateral Bounded Partial Denture Fabricated By Bre-Flex Versus Peek

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

Evaluation of the muscle activity of masseter in tooth borne partial denture wearers (class III modification 1 Kennedy's classification) with two different denture base materials (Breflex and PEEK) by means of electromyograph.

NCT ID: NCT03506685 Not yet recruiting - Clinical trials for Pain and Anterior Cruciate Ligament Reconstruction

Effectiveness of Dry Needling and STM on Pain Management for ACLR

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

The purpose of this study is to determine if dry needling (DN) and soft tissue mobilization (STM) is superior to standard treatment protocol for affecting pain, pain medication usage and measurements of range of motion (ROM) after ACL reconstruction surgery compared to a standard treatment protocol. Measurements of pain, pain medication usage, lower extremity functional scale (LEFS) and ROM will be taken day 2 post op and 1 week, 2 weeks, 3 weeks, and 4 weeks post op. It is hypothesized that the inclusion of DN and STM will acutely decrease the demand for pain medication and improve objective measurements when compared to a standard treatment protocol. Findings will potentially lead to insights as to the benefit of applying these interventions to help decrease the demand for pain medication post-surgery.

NCT ID: NCT03505970 Not yet recruiting - Clinical trials for Sports Nutritional Physiological Phenomena

Blood, Muscle and Exercise Responses to Sodium Bicarbonate Supplementation

Start date: August 2019
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the changes in activity of transporters of H+ (monocarboxylate transporters; MCT1, MCT4, NHE) following sodium bicarbonate supplementation and subsequent exercise performance. Fifteen healthy men (age 18-35 years) will be invited to attend the laboratory on five separate visits to a randomized, double-blind, placebo-controlled study. Participants will be supplemented with a 0.3 g/kg dose of sodium bicarbonate or placebo (Analytical Pharmacy, Brazil) in opaque gelatin capsules. One hour after supplementation they will perform a 1-km time trial and every 10 minutes a blood sample will be collected. A muscle biopsy will be taken prior to supplementation, immediately prior to exercise, and immediately post-exercise. A questionnaire will be also used to evaluate the side-effects associated with sodium bicarbonate supplementation. Muscle and blood samples will be analysed for acidity and H+ and muscle samples will be analysed for H+ transporters (MCT1, MCT4, NHE).

NCT ID: NCT03505931 Not yet recruiting - Clinical trials for Moderate or Severe Claudication (Rutherford Category 2 or 3)

Korean Multicenter Registry of ELUVIA Stent for Femoropopliteal Artery Disease (K-ELUVIA Registry)

Start date: May 2018
Phase:
Study type: Observational [Patient Registry]

- Prospective, multi-center single-arm observational study - A total of 100 subjects with femoropopliteal artery disease who meet all inclusion and exclusion criteria will be included. - Patients will be followed clinically for 12 months after the procedure. - An imaging study (duplex ultrasound, CT or catheter-based angiography) follow-up according to participating hospital's protocol will be performed at 12 months. - Ankle-brachial index, symptom status and presence of stent fracture will be evaluated at 12 months.

NCT ID: NCT03505242 Not yet recruiting - Clinical trials for Minimally Invasive Cardiac Surgery

Application of Bronchial Blocker in Minimally Invasive Cardiac Surgery

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

Both left single lung ventilation by left double lumen tube and bilateral ventilation with selective blockage of right middle lower lobe by bronchial blocker can provide suitable surgical field for minimally invasive cardiac surgery. The current study was designed to compare the impact of these two different methods on oxygenation, degree of pulmonary collapse and postoperative complications.

NCT ID: NCT03505073 Not yet recruiting - Clinical trials for Atherosclerotic Cardiovascular Disease

Association Between Dietary Habits and Risk Factors for Atherosclerotic Cardiovascular Diseases in Assiut Governorate

Start date: May 2020
Phase:
Study type: Observational [Patient Registry]

Studying and investigating the association between dietary habits and risk factors for atherosclerotic cardiovascular diseases in Assiut governorate

NCT ID: NCT03504969 Not yet recruiting - Clinical trials for Umbilical Cord; Complications, Affecting Fetus

Perinatal Outcomes in Umbilical Cord Entanglement

AssiutU
Start date: January 1, 2019
Phase:
Study type: Observational

Umbilical Cord Entanglement and Perinatal Outcomes.

NCT ID: NCT03504345 Not yet recruiting - Infertility Clinical Trials

Progesterone Supplementation in Frozen Embryo Transfer Cycles

Start date: May 2018
Phase: N/A
Study type: Interventional

Recurrent implantation failure (RIF) occurs after women undergo in vitro fertilization and have multiple embryos transferred but no resulting pregnancies. RIF is a very challenging clinical entity for the reproductive physician and the patient. In fact, there is not even an agreed upon definition in the medical community. Many potential causes have been investigated over the past several years but no clear answer has emerged. Interest has recently turned to the endometrium, or the lining of the uterus. Studies have shown that the genes that are turned on in the endometrium vary based on how long this tissue has been exposed to progesterone, an important hormone that prepares the uterine lining for implantation of the growing embryo. In some women, it seems that they require longer periods of progesterone exposure to reach the same state of readiness. We hypothesize that an even larger proportion of women in RIF population will require longer treatments with progesterone. In this study, we will randomize women with RIF who are about to undergo a frozen embryo transfer to one of two groups. The first group will have their embryo transfer done on the standard sixth day of progesterone treatment. The other group will have their transfer done on the seventh day of progesterone. We will be comparing the clinical pregnancy rate of the two groups as well as the live birth rate and miscarriage rate. We expect that extending the progesterone treatment by one day will increase the pregnancy rate of women with RIF.

NCT ID: NCT03504202 Not yet recruiting - Clinical trials for Patients With INOCA(Ischemia and no Obstructive Coronary Artery Disease) Who Have Coronary Microvascular Dysfunction

Effect of Trimetazidine on the Improvement of Coronary Microvascular Dysfunction in Patients With INOCA(Ischemia and no Obstructive Coronary Artery Disease)

T-MICRO
Start date: March 1, 2019
Phase: N/A
Study type: Interventional

This is a prospective study which aims to explore the effect of Trimetazidine on the improvement of coronary microvascular dysfunction in patients with INOCA (ischemia and no obstructive coronary artery disease). Enrolled patients will be assessed SAQ(Seattle Angina Score), Canadian Angina Grade(Canadian Cardiovascular Society, CCS), Six-Minute Walk Test, CFR(coronary flow reserve) .CFR inspection with D-SPECT and pressure guide wire.Patients will receive six months Trimetazidine(35mg tid) after enrollment. And their SAQ (Seattle Angina Score), Canadian Angina Grade(Canadian Cardiovascular Society, CCS), Six-Minute Walk Test, CFR will be followed up.