Clinical Trials Logo

Filter by:
NCT ID: NCT03078140 Completed - Pregnancy Related Clinical Trials

Iodine Supplement Strategies Between Routine Iodine Supplementation and Selective Iodine Supplementation

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Pregnant women who attend at our antenatal clinic will random to 2 groups. First will receive routine iodine supplementation. The other will receive iodinated pill or only iron supplementation base on their urine iodine status.

NCT ID: NCT03077555 Completed - Clinical trials for Ovulation Inhibition

Ovulation and Follicular Development Associated With Mid Follicular Phase Initiation of Combined Hormonal Contraception

Start date: January 21, 2017
Phase: Phase 4
Study type: Interventional

Quick starting combined oral contraception containing estradiol hemihydrate/nomegestrol acetate is effective to inhibit ovulation in healthy reproductive age women and non-inferiority to combined oral contraception containing ethinyl estradiol/gestodene.

NCT ID: NCT03077503 Completed - Clinical trials for Hemodynamic Response

Comparison of Dexmedetomidine and Fentanyl to Prevent Hemodynamic Response to Skull Pins Application

Start date: September 1, 2015
Phase: Phase 4
Study type: Interventional

To compare the effect between dexmedetomidine and fentanyl for controlling the hemodynamic response to skull pins application

NCT ID: NCT03077282 Completed - Healthy Volunteers Clinical Trials

Safety of Prasaprohyai 95%Ethanolic Extract Capsules in Healthy Volunteer

Start date: April 26, 2018
Phase: Phase 1
Study type: Interventional

To investigate the safety of Prasaprohyai 95% ethanolic extract at doses of 100 mg and 200 mg for for 6 weeks. (Clinical Trial phase I)

NCT ID: NCT03076398 Recruiting - Patient Compliance Clinical Trials

Development of Anaesthesia Electronic Medical Record

Start date: February 19, 2015
Phase: N/A
Study type: Observational

Normally, anaesthesia personnel make a record patients' information during the surgical procedure. Pre and post-operatively, they visit patients to make sure that their customers are well informed regarding the whole process and satisfied with the service as well as any complications that might be existed. The investigators would like to develop an anaesthesia electronic medical record at the point of care. The objectives are to record peri-operative patients' information in a real-time fashion, manage all administrative tasks as annual reports, and operate data as search engine for research and educational purpose.

NCT ID: NCT03075358 Completed - Uterine Bleeding Clinical Trials

Effects of Lidocaine Spray for Reducing Pain During Endometrial Aspiration Biopsy : a Randomized Controlled Trial

Start date: March 6, 2017
Phase: Phase 3
Study type: Interventional

Endometrial aspiration biopsy has been accepted as a diagnostic procedure of choice for women with abnormal uterine bleeding to examine endometrial pathology. The procedure has high accuracy comparing to conventional fractional curettage. However, it is associated with significant pain during the procedure. In general, there is no specific recommendation regarding the proper anesthesia used during the procedure. The aim of this study is to examine the effect of lidocaine spray for reducing pain during the endometrial aspiration procedure by comparing it with placebo and no intervention.

NCT ID: NCT03074994 Recruiting - Osteoarthritis,Knee Clinical Trials

The Comparative Efficacy of Peri-articular and Intraarticular Tranexamic Acid in Total Knee Arthroplasty

Start date: October 2016
Phase: Phase 2
Study type: Interventional

Post-operative bleeding in total knee arthroplasty (TKA) can result in hypovolemic shock and unnecessity for allogenic blood transfusions. Intravenous and topical tranexamic acid (TXA) have been well established in reducing blood loss postoperatively. However, there are lack of data on peri-articular TXA injection during TKA. Therefore, the investigators conducted a three-arm prospective, randomized, controlled trial to compare the effectiveness of bleeding reduction of peri-articular TXA injections, intraarticular TXA injections and control group.

NCT ID: NCT03072238 Completed - Clinical trials for Metastatic Prostate Cancer

Ipatasertib Plus Abiraterone Plus Prednisone/Prednisolone, Relative to Placebo Plus Abiraterone Plus Prednisone/Prednisolone in Adult Male Patients With Metastatic Castrate-Resistant Prostate Cancer

IPATential150
Start date: June 30, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of ipatasertib plus abiraterone and prednisone/prednisolone compared with placebo plus abiraterone and prednisone/prednisolone in participants with metastatic castrate-resistant prostate cancer (mCRPC).

NCT ID: NCT03071536 Recruiting - Clinical trials for Kidney Transplant; Complications

Furosemide Stress Test Predicting Early Graft Function in Kidney Transplantation

FOSTIK
Start date: November 25, 2016
Phase: N/A
Study type: Interventional

Furosemide is an old drug that has been used frequently in the postoperative period of kidney transplantation, aiming to achieve adequate urine output. There is no previous study that directly evaluate the urine response to standardized dose of furosemide in the postoperative period. The objective is to measure the urine output after standardized dose of furosemide is delivered, as a biomarker to predict the graft function in perioperative period.

NCT ID: NCT03068208 Not yet recruiting - Lichen Amyloidosis Clinical Trials

Efficacy of Methylene Blue Mediated Photodynamic Therapy for Primary Localized Cutaneous Amyloidosis Treatment in Asians

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Efficacy of Methylene blue mediated Photodynamic therapy for primary localized cutaneous amyloidosis treatment in Asians, pilot study.