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NCT ID: NCT04096521 Completed - Clinical trials for Folic Acid Deficiency

Serum Folic Acid Status, Genotyping MTHFR 677C-->T, Plasma Homocysteine, DNA Methylation of IGF2 Gene and Microbiota of the Children: Mother-Children Cohort Study

Start date: August 2, 2018
Phase:
Study type: Observational

This study is part of the East Jakarta Cohort Study to assess the current micronutrient status of the mothers and their children. The study also includes the assessment of genotyping of MTHFR 677C-->T of the mother and DNA methylation of IGF2 gene of the children.

NCT ID: NCT04085874 Completed - Obesity Clinical Trials

Effectiveness of Food-Based Recommendations for Minangkabau Women of Reproductive Age With Dyslipidemia

Start date: January 7, 2019
Phase: N/A
Study type: Interventional

This study aimed to assess effectiveness of promoting the optimized Food-based recommendations (FBRs) for improving dietary practices, nutrient intakes, nutritional status and lipid profile among Minangkabau women of reproductive age with dyslipidemia in a community setting. A cluster randomized community-based trial was conducted in Padang City, West Sumatra, Indonesia. Subjects are Minagabau women of reproductive age (20-44 y) with dyslipidemia. The subjects were assigned either into FBR group (n=48) that involved in 12-weeks prolonged contact of FBRs promotion or into non-FBR group, that received once nutrition counselling from usual standard of nutrition program. Baseline and end-line lipid profiles, nutritional status, dietary practice and nutrient intake data were assessed through biochemical assessment, anthropometri, and interview structured questionaire.

NCT ID: NCT04071379 Completed - Safety Clinical Trials

Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B

Start date: October 13, 2020
Phase: Phase 3
Study type: Interventional

Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) with Pentabio® vaccine Primed with Recombinant Hepatitis B

NCT ID: NCT04067687 Completed - Pediatric Cancer Clinical Trials

Home Visit Intervention in Pediatric Palliative Care

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

A randomized controlled trial to compare the quality of life between participants who were given palliative care (a 3-month home visit) and those who were not (intervention vs control group) was conducted. Participants consisted of children with cancer aged 2-18 years old. A two-way communication between a trained health worker and participants with or without their parents were conducted as the intervention (report by proxy or self-report). Interventions were given in 6 sessions (1 session every 2 weeks) focusing on problems solving education, symptoms management, self-care, communication, decision making, and long-term care plan assistance. In the first and twelfth week of the intervention, all participants were assessed with the Pediatric Quality of Life Inventory (PedsQLTM) questionnaire cancer module 3.0. Symptomps intensityof anorexia, sleep diturbance, and pain will be asessed in each visit. Participants were followed, Emergency Room (ER) admissions were recorded during follow up period. During the follow up period, ER admissions were recorded further.

NCT ID: NCT04059614 Completed - Clinical trials for Post Abdominal Surgery

Comparison of HFNC and COT to Diaphragm Function of Post-upper Abdominal Surgery Patients

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

This study aims to compare diaphragm thickness, air lung distribution, and several clinical and laboratory parameters on post abdominal surgery patients with conventional oxygen therapy vs high-flow nasal cannula

NCT ID: NCT04052165 Completed - Glaucoma Eye Clinical Trials

IOP Reduction and Complications of Polymethyl Methacrylate GDD on Glaucoma Patient

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Glaucoma is a group of diseases that damage the eye's optic nerve, result in progressive visual field defect and blindness. The aim of glaucoma management is to reduce IOP, and glaucoma implant surgery is the alternative treatment that can be chosen. The effectiveness of the implant on the end stage glaucoma patients was evaluated by the reduction of intra ocular pressure (IOP) and well formed blebs that were evaluated clinically and by using anterior scanning optical coherence tomography (AS-OCT). The safety of the implant was determined by the regression of the clinical symptoms and there were no severe complications such as implant extrusion. Two patients developed improvement of the visual acuity. This was an unpredictable positive result.

NCT ID: NCT04051268 Completed - Safety Issues Clinical Trials

Immunogenicity and Safety of Vi-DT (Diphtheria Toxoid) Typhoid Conjugate Vaccine (Phase III)

Start date: March 2, 2020
Phase: Phase 3
Study type: Interventional

Phase III study, Randomized, observer blind, lot to lot consistency, non inferiority to PQed typhoid conjugate vaccine and Typhoid Vi polysaccharide vaccine.

NCT ID: NCT04046289 Completed - Obesity Clinical Trials

Effects of Probiotics and Calcium Supplementation on Growth, Development, and Metabolic Parameters

PROBIOCAL
Start date: January 26, 2019
Phase:
Study type: Observational

Stunting is still a major problem in developing countries, including Indonesia, and has been associated with impaired development. Stunted children have also a higher risk of metabolic syndrome in adulthood. The gut microbiota, as a part of intestinal integrity, may promote intake of nutrient during childhood. Probiotics supplementation may optimize the balance of gut microbiota and further improve child growth during the window period. Furthermore, calcium could also improve child growth by increasing the resistance to intestinal infection. However, the long-term effects of gut microbiota optimization during childhood using probiotics and calcium on growth, development, and the metabolic condition has not widely studied.

NCT ID: NCT04029831 Completed - Analgesia Clinical Trials

Comparison of Different Ratio of Ketofol (6:1 vs. 4:1) for Sedation in Endoscopic Retrograde Cholangiopancreatography (ERCP)

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

Study was aimed to compare the effect of ketofol between 6:1 and 4:1 ratio in patients who underwent ERCP

NCT ID: NCT04029662 Completed - Undefined Clinical Trials

Reducing Pain Intensity During Spinal Needle Insertion: Valsalva Maneuver vs. Control Technique

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

This study was aimed to observe the efficacy of Valsalva maneuver in reducing pain intensity during spinal needle insertion.