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Central Jakarta, Indonesia Clinical Trials

A listing of Central Jakarta, Indonesia clinical trials actively recruiting patients volunteers.

RESULTS

Found (44) clinical trials

DLBS1442 for The Treatment of Pain in Patients Suspected Endometriosis

There will be three groups of treatment by dosage regimen in this study. Eligible subjects will be randomized to receive any of the following regimens: 1) DLBS1442 at a dose of 3 x 100 mg daily, or 2) DLBS1442 at a dose of 3 x 200 mg daily; or 3) ...

Phase

0.0 miles

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Prospective Single-arm Multi Centre Observations Ultimaster Des Registry

All consecutive patients suitable for treatment with DES according to hospital routine practice in centres across the world that agree to participate in the e-ULTIMASTER registry will be treated with Ultimaster DES. Secondary objectives Evaluation of worldwide utilization of DES, Detection of rare events in representative patient population, identification of ...

Phase N/A

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The Role of Platelet Rich Plasma Towards the Repair of Pelvic Floor Muscle Damage in Primipara

This study aims to see if platelet rich plasma (PRP) has beneficial effect on the repair of pelvic floor muscle damage in primipara. Therefore, this double blinded randomized clinical trial compares the pelvic floor muscle repair in primipara following labor between the interventional group who received intramuscular PRP injection in ...

Phase

0.0 miles

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Prenatal Administration of Spermine Promotes Maturation of Premature Fetal Gut Epithelial Tight Junction: Experimental Study on Fetal Rabbit

This experimental study is conducted with minimum 24 subjects which divided into 6 groups; 1) 24-days pregnant and is given prenatal spermine, 2) 26-days pregnant and is given prenatal spermine, 3) 28-days pregnant and is given prenatal spermine, 4) 24-days pregnant and is not given prenatal spermine, 5) 26-days pregnant ...

Phase N/A

0.22 miles

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DLBS1033 for Acute Ischemic Stroke Patients

Subjects in this study will be screened consecutively and eligible subjects will be randomized into two groups and receive the investigational drug, DLBS1033 at a dose of 490 mg three times daily or its placebo in addition to standard therapy for 28-days course of therapy. Standard therapy used in this ...

Phase

0.57 miles

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Transcranial Magnetic Stimulation (TMS) for Patients With Treatment Resistant Auditory Verbal Hallucination

Brief summary: This study will evaluate the effect of repetitive transcranial magnetic stimulation (rTMS) in schizophrenia with treatment resistant auditory hallucination Detailed description: Auditory verbal hallucinations in schizophrenia disorders have been proposed to be associated with a source- monitoring deficit. The improvement of the monitoring deficit will have major impact ...

Phase

0.57 miles

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A Trial Comparing Pain During Local Tumesent Injection In Fingers Using Different Syringe-Needle Combinations

METHODS 3.1 DESIGN This is a randomized, single-blinded controlled trial to measure local pain following local anesthesia tumescent injection using a different combination of syringe and needle in a healthy volunteer. 3.2 TIME AND PLACE The study will be conducted at Cipto Mangunkusumo Hospital (RSCM) in February to March 2018 ...

Phase N/A

0.88 miles

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The Effect of Andrographis Paniculata to GLP-1 Fasting Insulin Insulin 2-h Post OGTT and HOMA-IR

Blood's participants will be examined fasting plasma insulin and glycated albumin (from fasting blood) and insulin measured during a standardized 2-h OGTT, DPP-4 enzyme, and GLP-1 (from standardized 2-h OGTT blood). Then, complete urinalysis test. Participants will be randomized to be two groups are group have been intervenced by capsules ...

Phase N/A

0.97 miles

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Tranexamic Acid for The Treatment of Gastrointestinal Bleeding

This study is a randomized double-blind controlled trial study. Interventions were given in the form of tranexamic acid injection compared to placebo in patients with acute upper and lower gastrointestinal bleeding. Tranexamic acid were administered intravenously 1 gram loading dose, followed by 3 grams maintenance dose in infusion for 24 ...

Phase N/A

0.97 miles

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10 vs 14 Days Triple Therapy : H.Pylori Infection Eradication

This is a double-blinded randomized clinical trials, to determine the proportion of eradication of Helicobacter pylori infection using a triple therapy regimen for 10 days and 14 days. The triple therapy regimen was a proton pump inhibitor (Rabeprazole 20 mg twice daily), Amoxicillin 1000 mg twice daily, and Clarithromycin 500 ...

Phase

0.97 miles

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