Clinical Trials Logo

Filter by:
NCT ID: NCT04868474 Completed - Smoking Cessation Clinical Trials

Combining Default Choices and a Decision Aid to Improve Tobacco Cessation

FIRST
Start date: June 15, 2021
Phase: N/A
Study type: Interventional

The FIRST cluster randomized trial will evaluate the effect of 1) a training program encouraging general practitioners to offer smoking cessation treatment as a default choice to all current smokers consulting a general practitioner (GP), and 2) an interactive, electronic decision aid to guide smoking cessation treatment, on the proportion of current smokers seen in primary care who have quit smoking 6 months after a baseline visit to their GP, as compared to enhanced usual care.

NCT ID: NCT04868370 Completed - Clinical trials for Assessment of Arm and Hand Sensorimotor Functions in Multiple Sclerosis Subjects

Validation of a Novel Instrument Task for Assessing Upper Limb

Start date: May 5, 2021
Phase:
Study type: Observational

The aim of this study i to investigate a new approach (Physical Peg Insertion Test, PPIT) to measure sensorimotor function in the arm and hand. To achieve this, this novel approach will be compared with an existing approach (Virtual Peg Insertion Test, VPIT).

NCT ID: NCT04867746 Completed - Hamstring Rupture Clinical Trials

Clinical and Functional Outcomes at Least 2 Years After Hamstring Muscle Repair

HamRepair
Start date: December 2, 2020
Phase:
Study type: Observational

This study is to evaluate functional outcomes of a new, intraoperative lateral positioning of the anchors on the tuber ischiadicum, in comparison to regular anatomical anchoring direct on top of the tuber ischiadicumafter hamstring muscle repair. This study is to quantify at least 2 years postoperative functional, biomechanical and clinical outcomes including side-to-side differences in muscle strength, unipedal balance, gait, jumping and squatting function, muscle activity, in patients treated by hamstring muscle repair.

NCT ID: NCT04865757 Completed - Infarction Clinical Trials

Space Flap for Cerebral Protection Following Decompressive Hemicraniectomy for Stroke

Start date: July 2012
Phase: N/A
Study type: Interventional

In this study the investigators want to investigate to what extent the application of an artificial bone flape (space flap) influences the success of a decompressive craniectomy. In all participants, a space flap is placed immediately after removal of the skull cap. In a second operation, after 1-3 months, an operation is performed, in which the stored own skull bone is re-inserted. The artificial bone cover is removed at this point.

NCT ID: NCT04865653 Completed - Healthy Clinical Trials

LSD Base and LSD Tartrate Bioequivalence and Bioavailability in Healthy Subjects

LSD-Bio
Start date: March 17, 2022
Phase: Phase 1
Study type: Interventional

Lysergic acid diethylamide (LSD) is used as recreational substance and as a research substance to study the mind. Recreationally, LSD is typically used in the form of "blotters" containing LSD tartrate. In research, both LSD base (LSD alone) or LSD salt in the form of LSD tartrate are used. The oral bioavailability of LSD is not known and LSD alone and LSD as salt have never been directly compared regarding their equivalence of plasma concentrations and effects. Because different forms of LSD are used in research it is important to know their difference or equivalence for correct dosing of LSD. The present study will compare equivalent doses of LSD base in ethanol orally, LSD tartrate in water administered orally, LSD base in an orodispersible film administered orally and LSD tartrate in water administered intravenously, as well as a placebo using a double-blind, randomized, counterballanced cross-over design in healthy participants.

NCT ID: NCT04862013 Completed - Clinical trials for Anterior Cruciate Ligament Injuries

Return to Sports After ACLR

RTSACL
Start date: June 1, 2021
Phase:
Study type: Observational

Patients who were surgically treated with ACL reconstruction at a single clinic between 2013 and 2018 will be approached by a questionnaire regarding their return to sport after surgery. Questions will focus on the timepoint of the return, subsequent injuries, and the impact of the initial injury on the life of the patients. In addition, existing clinical data from the baseline visit and from the follow-up visits offered routinely to the patient will be used.

NCT ID: NCT04861831 Completed - Healthy Aging Clinical Trials

Power Centering for Seniors

PCS
Start date: January 29, 2021
Phase: N/A
Study type: Interventional

Walking difficulties, mobility decline and falls are prevalent among older adults. The incidence of each of these increases with age and the presence of each can negatively affect the quality of life in older adults. The purpose of this prospective clinical trial is to evaluate the efficacy of the Power Centering for Seniors multimodal, twice weekly, 12-week group intervention program to improve the mobility and quality of life in older, community-dwelling adults.

NCT ID: NCT04861155 Completed - Chronic Cough Clinical Trials

Validation and Evaluation of a Novel Cough Detection Device

Start date: April 22, 2021
Phase: N/A
Study type: Interventional

When diagnosing chronic cough (cough lasting longer than 8 weeks), the physician nowadays very often relies on the patient's narrative and description. In our research project we want to find out whether a cough detector can continuously and reliably record the cough, how the user-friendliness of the cough detector is assessed and whether this continuous recording can support the physician in his diagnosis.

NCT ID: NCT04854642 Completed - no Condition Clinical Trials

A Single Dose Study About the Influence of Food on the Oral Bioavailability of Ladarixin Capsule in Healthy Volunteers

Start date: October 20, 2020
Phase: Phase 1
Study type: Interventional

Primary objective: - to investigate the effect of food on the bioavailability of DF 2156Y after single dose administration of 400 mg of ladarixin to healthy male and female volunteers under fed and fasting conditions. Secondary objectives: - to investigate the effect of gender on the bioavailability of DF 2156Y and its metabolites (DF 2108Y and DF 2227Y) after single dose administration of 400 mg of ladarixin to healthy male and female volunteers - to evaluate safety and tolerability of a single dose administration of ladarixin 400 mg to healthy male and female volunteers.

NCT ID: NCT04849832 Completed - Iron-deficiency Clinical Trials

Effect of Polyphenols on Absorption of Iron From Sodium Iron Chlorophyllin

polySIC
Start date: June 21, 2021
Phase: N/A
Study type: Interventional

Polyphenols present in tea are known to inhibit the absorption of non heme iron. The inhibiting effect of tea on non-heme iron absorption is attributed to the flavonoids present in tea. It is well known that Ferrous sulfate is not absorbed well in the presence of polyphenols. We would like to evaluate the effect of polyphenols on the newly developed compound, sodium iron chlorophyllin (SIC), which mimics the heme iron structure. Comparisons of fractional absorption of SIC and Ferrous Sulfate in the presence of polyphenols can help identify the performance of the compounds as vehicles for iron delivery in the presence of iron absorption inhibitors. In a single-blind randomized cross-over study using stable iron isotope technique, iron bioavailability from SIC delivered with an inhibitory matrix can therefore be determined when given along with black tea