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NCT ID: NCT01651689 Enrolling by invitation - Alopecia Clinical Trials

Hair Counts From Vertical and Horizontal Sections of Scalp Biopsy SPecimens in Thai Population With Alopecia

ThaiScalpBx
Start date: October 2010
Phase: N/A
Study type: Observational

Hair disorders, expecialy scarring alopecia were diagnosed by scalp biopsy specimens in horizontal and vertical sections.(1-4) Data on hair density in Thais are lacking, although in Asians have more fewer hairs than whites.(5-7)Howevery, previous study from East Asian just had only one study and the data was more differently from West Asian and whites. Then this study was performed to evaluate hair density in Thais, and compared to previous study.

NCT ID: NCT01608698 Enrolling by invitation - Body Weight Changes Clinical Trials

Comparison of Body Weight Change During Contraception With Belara and Yasmin

Start date: June 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate different side effect in contraceptive use of two oral combined contraceptive pills (OCP)in combination of 30 mcg ethinylestradiol/2 mg chlormadinone acetate (Belara®) and 30 mcg ethinylestradiol/3 mg drospirenone (Yasmin®), especially body weight change.

NCT ID: NCT01500291 Enrolling by invitation - Depression Clinical Trials

A Study Survey of Stress in Anesthesia Personnel

stress
Start date: April 2012
Phase: N/A
Study type: Observational

It is inevitable that nearly both anesthesiologist and nurse anesthetist take a zero tolerance approach to avoidable safety problems in the provision of anesthesia. We would like to study the stress upon anesthesia personnel by using Suanprung Stress Test (SST) - a well-documented, psychological stress test, and Siriraj Anesthesia-related Stress Test (SAST) - a new developed open-ended opinion poll, to scrutinize the daily rounds stress and yield the solution to eradicate or alleviate those worries as well as improve both physical and mental health to handle the situation of difficulties.

NCT ID: NCT01496222 Enrolling by invitation - Clinical trials for Mild Cognitive Impairment

The Montreal Cognitive Assessment as a Screening Tool for Preoperative Mild Cognitive Impairment in Geriatric Patients

MoCA
Start date: January 2012
Phase: N/A
Study type: Observational

This is a prospective, double-blinded, control trial. The Montreal Cognitive Assessment is used to screen preoperative mild cognitive impairment in 582 consecutive geriatric patients, scheduled for general, vascular or urological surgery under general and/or regional anesthesia.

NCT ID: NCT01466309 Enrolling by invitation - Complication Clinical Trials

Efficacy of Adjustable Thermoplastic Oral Appliances in Patient With OSA

ThaiSomnoguard
Start date: July 2011
Phase: N/A
Study type: Interventional

Somnoguard, a titratable-thermoplastic oral appliances for the treatment of OSA, has been reported its safety and efficacy in Caucasians at least in the short-term. However, there has been no reports in Thai patients. The objectives of this study is to investigate its efficacy and safety in Thai patients with OSA.

NCT ID: NCT01273025 Enrolling by invitation - Oxidative Stress Clinical Trials

Lime Powder Regimen in Healthy Volunteers

LimePKphase1
Start date: December 2010
Phase: Phase 1
Study type: Interventional

The study aims to investigate the pharmacokinetic parameters and its antioxidative effects in Thai healthy men.

NCT ID: NCT01066351 Enrolling by invitation - Acute Renal Failure Clinical Trials

Efficacy of Erythropoietin to Prevent Acute Kidney Injury in Chronic Kidney Disease Patients Undergoing Cardiac Surgery

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the efficacy of erythropoietin for prevention acute kidney injury in CKD patients undergoing cardiac surgery.

NCT ID: NCT01061320 Enrolling by invitation - Clinical trials for Contrast Induced Nephropathy

Efficacy of Alpha Tocopherol for Prevention of Contrast-induced Nephropathy in Chronic Kidney Disease (CKD) Patients

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the efficacy of alpha tocopherol for prevention contrast-induced nephropathy in CKD patients undergoing elective coronary procedures.

NCT ID: NCT01017471 Enrolling by invitation - Clinical trials for Carpal Tunnel Syndrome

Carpal Tunnel Syndrome Release Using PSU Retractor

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The investigators study aims to evaluate both efficacy and safety of carpal tunnel release using limited incision with the PSU retractor compared to standard incision. The investigators will do a randomized controlled trial in 60 patients with carpal tunnel release and evaluate for outcome regarding pain, VAS score, return to work time, CTS score and complications at 6 months.

NCT ID: NCT01017445 Enrolling by invitation - Knee Osteoarthritis Clinical Trials

Stick Versus Quadricep Exercise for Knee Osteoarthritis

Start date: October 2007
Phase: Phase 3
Study type: Interventional

This study aims to compare the efficacy between Boonme stick exercise and quadriceps strengthening exercise in knee osteoarthritis.Patients diagnosed as knee osteoarthritis using Altman criteria will be randomized into 2 groups using simple random technique. Patients will be instructed and trained for both quadriceps or Boonme stick exercise by one-trained physical therapist. All patients will be treated with behavioral modification, NSAIDs and analgesic drugs and regularly follow-up . Assessment included visual analogue scale, exercise compliance, WOMAC and patient satisfaction were done by an assessor in a blinded fashion.