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NCT ID: NCT05059509 Completed - Atopic Dermatitis Clinical Trials

Evaluate Efficacy of FB825 in Adults With Atopic Dermatitis

Start date: February 6, 2020
Phase: Phase 2
Study type: Interventional

This is an open labeled exploratory study to evaluate efficacy of FB825 in adults with atopic dermatitis (AD). The study will be conduct at one medical center in Taiwan. Approximately 20 subjects with atopic dermatitis (AD), who meet the criteria for study entry, will be enrolled to the study. All eligible subjects will receive FB825, 5mg/kg, by 1 hour IV infusion on Day 1. Subjects will return to the study site on Days 15, 29 and 57 for the safety and efficacy evaluation. Subjects who premature withdraw from the study will have an end of study (EOS) visit within 7 days.

NCT ID: NCT05059119 Completed - Clinical trials for Locally Advanced Cervical Cancer

Rectovaginal Fistula in Post-Radiotherapy Advanced Cervical Cancer Patients

Start date: September 1, 2020
Phase:
Study type: Observational

To investigate the associated risk factors of rectovaginal fistula

NCT ID: NCT05056974 Completed - HIV-1 Infection Clinical Trials

A Proof-of-concept Trial to Evaluate the Safety and Efficacy of UB-421 Plus Chidamide in Changing HIV Reservoirs

Start date: December 2, 2021
Phase: Phase 2
Study type: Interventional

This is a phase II proof-of-concept trial study to assess the safety and efficacy of UB-421 monotherapy plus chidamide in changing the latent HIV reservoir among ART-treated HIV-1 adults with stably viral suppression who undergo ART interruption.

NCT ID: NCT05053542 Completed - Pain, Postoperative Clinical Trials

The Necessity of Preoperative Bowel Preparation

Start date: March 1, 2020
Phase:
Study type: Observational

Hemorrhoidectomy is an common treatment for high-grade hemorrhoids. The necessity of preoperative bowel preparation (PBP) in hemorrhoidectomy is inconclusive. This study aims to evaluate the benefit and safety of PBP in hemorrhoidectomy.

NCT ID: NCT05052138 Completed - Loneliness Clinical Trials

Effects of Tactile Massage in Long-Term Care Facilities

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

The older residents in the long-term care facilities frequently experience loneliness, anxiety, and depressive symptoms. Improving residents' psychological health problems is one of the important tasks for nursing staff. Individual experiences a sense of security and feels of being cared for after tactile massage (TM).The randomized controlled trial research design and convenience sampling will be employed. Through skin-to-skin contact, the oxytocin can be induced to make individual feel relaxed, reduce anxiety, and feel pleasure. The randomized controlled trial research design and convenience sampling will be employed. The eligible residents will be randomly assigned to intervention group and comparison group (usual care). The intervention group will receive two 15-min tactile massages per week for 4 weeks. The comparison group will receive regular care and activities.

NCT ID: NCT05051306 Completed - Clinical trials for Inflammatory Response

Effects of Resistance Exercise on Metabolic Responses

Start date: February 18, 2021
Phase: N/A
Study type: Interventional

Healthy young adults will complete three trials in a randomized crossover counter-balanced order, including two different loads of resistance exercise and sedentary control. During each trial, blood samples will be collected. The investigators hypothesized that high-load and low-load resistance exercise exert similar metabolic responses.

NCT ID: NCT05049408 Completed - Clinical trials for Oral Squamous Cell Carcinoma

Verification of Saliva MMP-1 as a Diagnostic Marker of Oral Cavity Cancer

Start date: February 17, 2011
Phase:
Study type: Observational

The study is designed to measure salivary matrix metalloproteinase-1 (MMP-1) using the enzyme-linked immunosorbent assay (ELISA) we developed previously in patients with oral potentially malignant disorders (OPMD), oral squamous cell carcinoma (OSCC), and healthy participants. The purpose of this study is to evaluate the potential of the newly developed salivary MMP-1 ELISA as an adjunctive tool to aid in diagnosis of OSCC.

NCT ID: NCT05049213 Completed - Covid19 Clinical Trials

Effect of Local Treatment(Carrageenan Nasal Spray and PVP-I Mouthwash) in Reducing Viral Load in Patients With COVID-19

LT-COVID19
Start date: June 24, 2022
Phase: Phase 4
Study type: Interventional

The goal of this study is to recruit confirmed Covid-19 patients, to evaluate whether the topical anti-septic can improve clinical outcome in early Severe acute respiratory syndrome coronavirus 2(SARS-CoV-2) infection. During the global pandemic period, an effective and highly available method once be identified, it will reduce the risk of disease transmission and lower the medical burden.

NCT ID: NCT05048849 Completed - Covid19 Vaccine Clinical Trials

A Study to Evaluate the Safety, Tolerability, and Immunogenicity of COVID-19 Vaccine, CT-COV-21 Extension Study

Start date: July 19, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and immunogenicity of MVC-COV1901 vaccine who are generally healthy or with stable pre-existing health conditions and have received 2 doses of Placebo in the main study CT-COV-21

NCT ID: NCT05048173 Completed - Lymphadenectomy Clinical Trials

Sentinel Lymph Node Biopsy Versus Lymphadenectomy in Endometrial Cancer

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

To compare sentinel lymph nodes biopsy versus comprehensive lymphadenectomy in patients with early stage endometrial cancer.