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NCT ID: NCT04840329 Completed - Endometriosis Clinical Trials

Endocation: Trial of an Endometriosis Education Program

Start date: April 9, 2021
Phase: N/A
Study type: Interventional

Endometriosis is a common condition that affects 10% of females, causing chronic pain and other health concerns. Currently, it takes 8-12 years to be diagnosed with endometriosis, in part because there is low awareness of this condition. This research is designed to test whether providing endometriosis education in schools can help increase early awareness of the condition.

NCT ID: NCT04840147 Recruiting - Clinical trials for Articular Cartilage Disorder of Knee

A Comparison of JointRep® and Microfracture in Repair of Cartilage Lesions on the Femoral Condyle or Trochlea,

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

The aim of the study is to compare whether JointRep® plus microfracture is more effective than microfracture alone when treating symptomatic focal articular cartilage lesions in the knee (femoral condyles or trochlea).

NCT ID: NCT04840121 Completed - Fertility Clinical Trials

Personalizing Window of Implantation During Frozen Embryo Transfer

AdhesioRT
Start date: March 24, 2021
Phase: N/A
Study type: Interventional

Embryo implantation is a crucial event in the establishment of a pregnancy. Although the clinical and culture conditions to obtain a "good quality" embryo are well advanced today, endometrial receptivity remains a major barrier in assisted reproductive techniques. Once a high-quality embryo is transferred, impaired uterine receptivity is believed to be one of the major reasons behind failure of the establishment of pregnancy.

NCT ID: NCT04839380 Completed - Atopic Dermatitis Clinical Trials

The Purpose of the Study is to Evaluate the Effect of Ruxolitinib Cream on Itch in Participants With Atopic Dermatitis

SCRATCH-AD
Start date: October 12, 2021
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the effect of ruxolitinib cream on itch in participants with Atopic Dermatitis.

NCT ID: NCT04838899 Recruiting - Clinical trials for Castration-Resistant Prostate Cancer

Stereotactic Ablative Radiation Therapy for Abiraterone-Resistant, Oligoprogressive Metastatic Prostate Cancer

Start date: July 16, 2016
Phase: N/A
Study type: Interventional

There is increasing worldwide interest in exploring stereotactic ablative body radiotherapy (SABR) for treating metastases in men with prostate cancer, including for the treatment of oligoprogressive metastases. The latter applies to a situation whereby patients with widespread metastases undergoing systemic therapy present with a solitary or a few metastatic tumors that progress, while all other metastases are stable or responding. The usual practice would be to change systemic therapy at this point, but another approach is to locally ablate the "rogue" metastases and continue the same systemic therapy. SABR used in this scenario may delay the need to switch to another line of systemic therapy and improve progression-free survival while patients stay on the same systemic therapy.

NCT ID: NCT04838808 Completed - Clinical trials for Type II Myocardial Infarction

Rivaroxaban in Type 2 Myocardial Infarctions

R2MI
Start date: April 5, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This trial is the pilot phase of a randomized controlled trial to test the feasibility of recruiting patients with a type 2 myocardial infarction and randomizing them to low-dose rivaroxaban to reduce the risk of major cardiovascular events.

NCT ID: NCT04838782 Recruiting - Clinical trials for Recurrent Glioblastoma

Role of Repeat Resection in Recurrent Glioblastoma

Start date: August 26, 2021
Phase: N/A
Study type: Interventional

Patients with recurrent Glioblastoma (GBM) are commonly presented to surgeons, along with the question of whether or not to re-resect the recurrence. There is no Level 1 evidence to support a role for repeat surgery in this context, but a multitude of observational research suggests that repeat surgery may improve quality survival. Unfortunately, these studies all suffer from selection bias. The goal of this study is to provide a care trial context to help neurosurgeons manage patients presenting with recurrent GBM, with no additional risks, tests, or interventions than what they would normally encounter in routine care. Secondary goals include a test of the hypothesis that repeat resection can improve median overall survival, and that it can increase the number of days of survival outside of a hospital/nursing/palliative care facility.

NCT ID: NCT04838561 Completed - Type 1 Diabetes Clinical Trials

Assessing the Impact of Control-IQ Technology

Start date: March 15, 2021
Phase:
Study type: Observational

This is a single-centre, mixed-methods, prospective study in pediatric patients with T1D initiating Control-IQ technology on the Tandem t-slim X2 insulin pump. Primary Objective: To determine pediatric T1D patients' and their parents' perceptions of the impact of Control-IQ on their psychosocial functioning and quality of life.

NCT ID: NCT04838353 Active, not recruiting - Heart Failure Clinical Trials

Alleviate-HF-2 Study

Start date: April 3, 2021
Phase: N/A
Study type: Interventional

Patients with heart failure and preserved left ventricular ejection fraction (HFpEF, EF ≥ 50%) or mid-range left ventricular ejection fraction (HFmrEF, 40% < EF < 50%) with mild to moderate functional limitation will be evaluated for treatment via creation of a no-implant interatrial shunt using clinical, echocardiographic, and invasive hemodynamic data

NCT ID: NCT04838197 Completed - Caregiver Burnout Clinical Trials

Understanding Caregiver Burden for Hip and Knee Replacement Surgery Patients

Start date: March 3, 2022
Phase:
Study type: Observational

Caregiver burden is the response to the emotional, financial, physical, psychological, and social stressors associated with having to care for another family member. Previous studies have looked at the impact of caregiver burden in caregivers caring for loved ones dealing with long-term disease, such as dementia. The research has found that one in three caregivers suffer from depression, and experience high levels of stress and anxiety. However, these findings may not be relatable to the outpatient surgical setting. The purpose of this study is to find out how various factors such as the physical, emotional, social, and financial burden impact caregivers who are responsible for providing care to patients who are undergoing same-day surgical procedures that are traditionally performed as inpatient surgery. By understanding this potential burden on the caregiver, we hope that future healthcare improvements can be made to minimize this impact on the patients and their caregiver.