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NCT ID: NCT06175962 Enrolling by invitation - Menopause Clinical Trials

Perımenopausal Women's Attıtudes Towards Menopause and Spırıtual Well-Beıng

Start date: December 20, 2023
Phase: N/A
Study type: Interventional

Menopause; cessation of menstruation due to cessation of follicular activity is the transition from the reproductive period to non-reproductive life. Considering that the average life expectancy is increasing, women spend most of their lives in the menopausal period. Women who have a positive attitude towards menopause have a positive body image, experience less depressive experiences, and the severity of menopause symptoms decreases. It has also been assumed that spiritual well-being is effective in reducing the severity of menopause symptoms and anxiety, supporting positive body image, and coping with losses. Baduanjin exercise is a type of body mind exercise. It increases the production of life energy and distributes it to different aspects of the body. It is thought that the baduanjin body-mind exercise to be applied to perimenopausal women will have positive effects on the spiritual well-being of menopausal women and their attitudes towards menopause. Thus, it is expected that women's transition and adaptation to the menopause process will be easier.

NCT ID: NCT06412445 Enrolling by invitation - Inguinal Hernia Clinical Trials

Self-Fixating Mesh Versus Mesh Fixation With Tissue Glue in Laparoscopic Inguinal Hernia Repair

Start date: December 20, 2023
Phase: N/A
Study type: Interventional

The main objective of this study is to compare between the safety and efficacy of self-fixating mesh versus mesh fixation with tissue glue in patients undergoing laparoscopic transabdominal inguinal hernia repair (TAPP). The criteria of comparison shall include operating time, post-operative pain and recurrence.

NCT ID: NCT00884455 Enrolling by invitation - Clinical trials for Alpha 1 Antitrypsin Deficiency

Alpha-1 Foundation DNA and Tissue Bank

Start date: December 2002
Phase:
Study type: Observational

This is a long-term follow-up banking protocol that collects medical information and tissue (blood, liver and lung) samples for future research; use of data and samples for research purposes is overseen by the Tissue Bank Advisory Committee; the purpose of the Bank is to further research on alpha-1 antitrypsin deficiency.

NCT ID: NCT00600652 Enrolling by invitation - Healthy Clinical Trials

FCM Analysis GR in Steroid-Treatment Patients

Start date: December 2006
Phase: N/A
Study type: Observational

Monitoring the GR with a GR-MoAb and FITC-Dex probes by FCM would be useful and convenient in determination GR before the steroid treatment in clinical, especially in steroid resistant states, in order to design more efficient clinical treatment protocols.

NCT ID: NCT00863837 Enrolling by invitation - Clinical trials for Esophageal Variceal Rebleeding

Prevention of Esophageal Variceal Rebleeding

Start date: December 2006
Phase: Phase 4
Study type: Interventional

BACKGROUND: Previous studies showed that the combination of endoscopic therapy with vasoconstrictor is better than either vasoconstrictor or endoscopic therapy alone in achieving the successful hemostatsis of acute variceal bleeding. The rationale of using vasoconstrictor is to enhance the efficacy of hemostasis by endoscopic therapy. Nowadays, endoscopic variceal ligation (EVL) has replaced endoscopic injection sclerotherapy (EIS) as the endoscopic treatment of choice in the arresting of acute esophageal variceal hemorrhage. EVL alone can achieve hemotasis up to 97% even in cases of active variceal hemorrhage. However, early rebleeding due to ligation-induced ulcer may be encountered. It appears that prevention of esophageal ulcers and bleeding by a proton pump inhibitor may be more logical than using a vasoconstrictor after cessation of bleeding by EVL. Thus, the investigators designed a controlled trial to compare the initial hemostasis, early rebleeding rate in cirrhotic patients presenting with acute variceal bleeding receiving either emergency EVL plus vasoconstrictor infusion or losec infusion for 5 days.

NCT ID: NCT00550524 Enrolling by invitation - Knee Osteoarthritis Clinical Trials

Stem Cell Transplantation for the Treatment of Knee Osteoarthritis

Start date: December 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find if autologous stem cell transplantation can improve clinical manifestations of knee osteoarthritis.

NCT ID: NCT00564538 Enrolling by invitation - Clinical trials for Liver Transplantation

A Study of Thymoglobulin and Tacrolimus in Liver Transplant

thymo
Start date: December 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare kidney function, long term patient and graft survival, and incidence of acute rejection in liver transplant recipients between one group receiving thymoglobulin induction and delayed initiation of tacrolimus and another group of liver transplant recipients having immediate administration of tacrolimus without any induction immunosuppression.

NCT ID: NCT00606385 Enrolling by invitation - Clinical trials for Hepatocellular Carcinoma

Prospective Randomized Trial of Laparoscopic Versus Open Liver Resection for HCC

HCC
Start date: December 2007
Phase: N/A
Study type: Interventional

Short-term outcomes of laparoscopic liver resection is better than those of open liver resection Laparoscopic liver resection is better than open resection in immunological aspects

NCT ID: NCT00623116 Enrolling by invitation - Kallmann Syndrome Clinical Trials

A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland

Start date: December 2007
Phase: N/A
Study type: Interventional

Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

NCT ID: NCT00639652 Enrolling by invitation - Clinical trials for Carcinoma, Basal Cell

Recurrence Rate and Esthetic Outcome After Excision of Basal Cell Carcinomas Excluded From Trial NCT00515970

Start date: December 2007
Phase: N/A
Study type: Observational

Currently, we conduct a prospective, randomized trial comparing the outcome of surgical excision with the outcome of curettage in nodular and superficial BCCs. Larger BCCs and micronodular or sclerosing BCCs are not included in the randomized study. They are mainly operated using three-dimensional histology (3D-histology, micrographic surgery). In this observational study we measure the cosmetic result and the recurrence rate of all BCCs not included in the randomized trial.