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NCT ID: NCT05862428 Completed - Clinical trials for Intraoperative Blood Loss

Rectal Misoprostol in Women Undergoing Total Abdominal Hysterectomy for Intraoperative Blood Loss Reduction

Start date: February 18, 2022
Phase: N/A
Study type: Interventional

Comparing of the intraoperative blood loss between group rectal misoprostol group and control group

NCT ID: NCT05862376 Completed - Iodine Deficiency Clinical Trials

Nutritional Status and Iodized Salt Use Among School-aged Children

Start date: April 1, 2021
Phase:
Study type: Observational

To determine and explore the iodized salt concentration provided in the local community, especially in the Phu Kut district whether it meets the standard or not. This district is located in a mountainous area which means that the local community confronts with geographical access due to the limited transportation and road condition, in addition, it is quite far from downtown approximately 26 kilometers and it is difficult to access the iodized salt consumption. On the other hand, since 2013, the Lao People's Democratic Republic has implemented the iodized survey of urine among the primary students, this time could be the chance to compare based on the previous data, which will be an important source of the data for certifying the quality of iodized salt available in the local community that could be one cause of lacking iodized salt intake. Furthermore, the investigators could conduct the survey and monitor the current action plan related to iodized consumption in Laos as well, in order to eradicate diseases concerning with lacking iodized salt intake. Objectives 1. To investigate the nutritional status of school-aged children (SAC) living in Phu Kut City, Xieng Khouang province. 2. To investigate the iodine status and iodized salt use of school-aged children (SAC) living in Phu Kut City, Xieng Khouang province.

NCT ID: NCT05857475 Completed - COPD Clinical Trials

Efficacy of CPAP Therapy on Pulmonary Function Test in Patients With COPD-OSA Overlap Syndrome

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

To evaluate efficacy of CPAP Therapy on Pulmonary Function Test in Patients With COPD-OSA Overlap Syndrome

NCT ID: NCT05826899 Completed - Bioavailability Clinical Trials

A Stable Isotope Study to Evaluate the Bioavailability of an Oat Protein-based Iron Delivery System

Start date: April 3, 2023
Phase: N/A
Study type: Interventional

In the current study, the OAT fibril - Fe SA (Fe-oat 1) and OAT fibril - Fe NaOH (Fe-oat 2) will both be studied in vivo, alone are oat fibril powder add iron supplement is soluble in water and oat fibril powder add iron supplement is soluble in water in a food matrix (acai puree and honey) to assess their promise as Fe food fortificants. This first in human study to bioavailability assessment and adverse effect of the OAT fibril - Fe SA (Fe-oat 1), OAT fibril - Fe NaOH (Fe-oat 2) and in a food matrix to assess their promise as Fe food fortificants. This study will be conducted with the following objectives. 1. To conduct a stable Fe isotope study to evaluate the bioavailability of OAT-Fe formulated using two reducing agents (Fe-oat 1 and Fe-oat-2) and compared to FeSO4. 2. To compare the performance of Fe-oat 1 and 2 in a food matrix containing Fe inhibitors, (acai puree and honey) in comparison to FeSO4 in a similar meal matrix.

NCT ID: NCT05813119 Completed - Diagnosis Clinical Trials

Efficacy of Digital Otoscope and Otoendoscope for Diagnosis of Middle Ear Pathology

otoscopy
Start date: July 1, 2022
Phase:
Study type: Observational

For diagnosis of external and middle ear diseases, an otoscope is a key instrument to use. A microscope has been used as a reference standard to confirm pathology. An endoscope has been also widely used. Both microscope and endoscope provide an excellent image quality, can record and capture the images, and the images can be visualized with an export system. A digital otoscope is widely available and more affordable. A comparative study of the efficacy of the endoscope and the digital endoscope will be performed.

NCT ID: NCT05808556 Completed - High Blood Pressure Clinical Trials

Sticker Pad Containing Essential Oil in Volunteer With High Blood Pressure

Start date: October 2, 2020
Phase: N/A
Study type: Interventional

The aims of the study were to evaluate efficacy and safety of the sticker pads containing lavender and ylang ylang oil in high blood pressure volunteers

NCT ID: NCT05802927 Completed - Clinical trials for Diabetes Mellitus, Type 2

Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes

Start date: July 5, 2023
Phase: N/A
Study type: Interventional

A randomized, controlled, crossover design with three treatments to determine the effects of diabetes-specific formula on glycemic control in individuals with type 2 diabetes.

NCT ID: NCT05791266 Completed - Healthy Clinical Trials

Safety of Sticker Pad Containing Essential Oil Containing Lavender and Ylang-ylang Oil

Start date: March 21, 2022
Phase: N/A
Study type: Interventional

The aims of the study were to evaluate safety of sticker pads containing lavender and ylang ylang oil in healthy volunteers.

NCT ID: NCT05779046 Completed - Allergic Rhinitis Clinical Trials

Acute Effect of High Intensity Interval Exercise in Patients With Allergic Rhinitis

Start date: September 10, 2022
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the acute effect of high intensity interval exercise on respiratory function and rhinitis symptoms in allergic rhinitis patients.

NCT ID: NCT05758090 Completed - Analgesia Clinical Trials

Newborn Infant Parasympathetic Evaluation (NIPE) for Guiding Intraoperative Fentanyl in Children Under 2 Years

Start date: March 10, 2023
Phase: N/A
Study type: Interventional

During general anesthesia, objective monitoring for analgesia is still lacking. The administration of opioids relies on the experience of the anesthesiologist. There are some monitors, e.g., Analgesia Nociception Index (ANI), showing that they can evaluate analgesia in adults. Recently, a Newborn Infant Parasympathetic Evaluation (NIPE) monitor was released for assessing analgesia in children with age less than 2 years. The investigators aim to assess the efficacy of NIPE as a guide for intraoperative fentanyl administration in children under 2 years.