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NCT ID: NCT06287424 Completed - Periodontitis Clinical Trials

The Efficacy Of AGE On Periodontitis

Start date: April 4, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to assess the long-term efficacy of "AGE among on deep periodontal pockets by different doses of "AGE" for a period of 18 months.

NCT ID: NCT06282276 Completed - Weight Stigma Clinical Trials

Anti-fat Attitudes and Weight Stigma Among Orthopedic Surgeons

Start date: October 1, 2022
Phase:
Study type: Observational

Evidence shows that anti-fat attitudes and weight stigma are prevalent among healthcare professionals and may affect treatment decisions regarding patients with obesity. The present study aimed to examine the presence of anti-fat attitudes and weight stigma among orthopedic surgeons and their correlation to the therapeutic approach to patients with obesity. In this cross-sectional survey, 150 orthopedic surgeons will complete a web-based questionnaire. the questionnaire is based on Antifat Attitudes Questionnaire (AFA), developed by Crandall in 1994. In addition, the questionnaire will include a questionnaire developed by Bocquier in 200521 to explore weight stigma among physicians.

NCT ID: NCT06251596 Completed - IVF Clinical Trials

What is the Impact of Frozen Embryo Transfer Protocol, on Endometrial Compaction

Start date: January 25, 2021
Phase:
Study type: Observational

This study aims to evaluate endometrial thickness on the day of the frozen embryo transfer, compared to endometrial thickness on the last day of assessment of the endometrium before exposure to progesterone in respect to the protocols used for endometrial preparation

NCT ID: NCT06224972 Completed - Sleep Disorder Clinical Trials

Evaluation of the Usability and Performance Assessment of the DormoTech VLAB Device as a Home Sleep Test

Start date: June 13, 2023
Phase:
Study type: Observational [Patient Registry]

The study is a comparative, self-controlled, randomized, prospective investigation designed to assess the usability and accuracy of the DormoTech Vlab and compare its performance with a full polysomnography (PSG) study conducted over one night in a sleep lab. For the purpose of this study, the selected PSG device used for comparison is the Nox A1 system (K192469). Participants were required to wear the DormoTech Vlab, answer questionnaires pre and post-study, and simultaneously undergo a full PSG test using the Nox system. The statistical methodology for this study was designed to ensure a comprehensive analysis of the data, adhering to the standards set by the International Council for Harmonisation (ICH) E3 guideline

NCT ID: NCT06217952 Completed - Cystic Fibrosis Clinical Trials

Safety, Tolerability, and Pharmacokinetics of SPL84 in Healthy Volunteers

Start date: February 5, 2023
Phase: Phase 1
Study type: Interventional

This Phase 1 study evaluated the safety, tolerability, and pharmacokinetics of SPL84 single ascending doses (SAD) in healthy volunteers (HV)

NCT ID: NCT06205134 Completed - Anaphylaxis Clinical Trials

Comparative Bioavailability of Intranasal Epinephrine

Start date: August 22, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

A Study to Compare the Bioavailability of Epinephrine following a Single Nasal Dose of FMXIN002 Microspheres Powder 3.6 mg, and 4mg with EpiPen 0.3mg Intramuscular Injection in Healthy Adults

NCT ID: NCT06204575 Completed - Clinical trials for Dementia With Lewy Bodies

Focused Ultrasound Thalamotomy for Tremor Relief in Atypical Parkinsonism

FUSAP
Start date: November 1, 2013
Phase:
Study type: Observational

The goal of this retrospective observational study is to describe the efficacy of focused ultrasound ventral-intermediate nucleus thalamotomy in patients with atypical parkinsonism. - Is this treatment efficacious in patients with multiple system atrophy? - Is this treatment efficacious in patients with diffuse Lewy Body Dementia? Data will be collected from patients charts.

NCT ID: NCT06196359 Completed - Rehabilitation Clinical Trials

Assessing Function and Pain After Total Knee Arthroplasty With Combined Femoral and Popliteal Nerve Block

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

The goal of this interventional study is to examine whether a pain management technique of combined femoral and popliteal nerve block is effective in total knee arthroplasty patients. The main questions it aims to answer are: Are there differences in postoperative outcomes? Does the nerve block, age, preoperative quadriceps muscle strength and Oxford Knee Score of the patient predict early functional ability? Participants underwent total knee arthroplasty and assessments. Researchers compared pain management techniques to assess effects on postoperative outcomes and identified the importance of preoperative variables a predictors of early functional ability. Further research is required to refine postoperative pain management strategies.

NCT ID: NCT06184087 Completed - Childbirth Classes Clinical Trials

Childbirth Education on Upright Positions Mobility During Labor

Start date: November 21, 2020
Phase: N/A
Study type: Interventional

Background and study aims: A prospective quasi-experimental study will be conducted among nulliparous women from the ultra-orthodox Jewish community. Study design: While the control group participated in routine childbirth education, the intervention group learned with childbirth education that included interactive and constructive cognitive engagement activities. Participants in both groups completed a set of questionnaires regarding knowledge, attitudes, and self-efficacy.

NCT ID: NCT06160570 Completed - Rectal Cancer Clinical Trials

IMRT Versus 3DCRT for Locally Advanced Rectal Cancer, Prospective Phase II Study.

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The goal of this prospective phase II study was to determine whether personalized planning-based nCRT for LARC would indeed decrease small bowel dose, and whether selected plans, specifically prioritizing lower dose to small bowel, would result in lower rates of acute GI toxicity compared with previously reported rates.