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NCT ID: NCT05456698 Not yet recruiting - Clinical trials for Acute Lymphocytic Leukemia

Efficacy and Safety of Inotuzumab Ozogamicin in Treating Adult Patients With Ph Negative ALL With Minimal Residual Disease Positive After Induction Chemotherapy

Start date: August 1, 2022
Phase: Phase 2
Study type: Interventional

A single-center, single-arm, open-label, interventional, phase II clinical trial to evaluate the efficacy and safety of InO in B-ALL achieved CR/CRi after 1L induction chemotherapy with positive minimal residual disease.

NCT ID: NCT05457452 Not yet recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Functional Outcomes Comparison in Patients Using Knee Brace Post ACL Reconstruction With Autograft Bone Quadricep Tendon

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

This study is a study looking for the relationship between variables with a prospective cohort design to determine functional outcomes subjectively and objectively in patients with and without braces after ACL reconstruction with bone quadriceps tendon per arthroscopy.

NCT ID: NCT05459727 Not yet recruiting - Clinical trials for Cardiovascular Diseases

Effects of Non-surgical Periodontal Therapy on Cardiovascular Risk

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

This study is to evaluate whether non-surgical periodontal therapy can help to control the cardiovascular risk among patients with moderate/severe periodontitis and at risk of cardiovascular disease.

NCT ID: NCT05459766 Not yet recruiting - Clinical trials for Total Knee Arthoplasty

Effects of a Perioperative Action Observation and Motor Imagery Training in Patients Undergoing Total Knee Arthroplasty

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

The study is aimed at investigating the effects of action observation and motor imagery training in patients undergoing total knee arthroplasty. Fifty participants will be enrolled during hospital admission and randomized into 2 groups (AO+MI and CTRL groups). AO+MI will undergo 12-minute AO+MI intervention for 3 days (preoperative day, first and second postoperartive days), whereas CTRL group will undergo usual care. At baseline, first and third postoperative days, participants will be assessed for mobility, pain, range of motion, quadriceps acrivation failure and patient's bady-pain representation by a blinded operator.

NCT ID: NCT05460819 Not yet recruiting - Breast Cancer Clinical Trials

Acupuncture for Hot Flashes in Patients With Hormone Receptor-positive Breast Cancer.

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

This study intends to further evaluate the efficacy of acupuncture by comparing the intervention effects of different acupuncture treatment regimens on hot flashes in breast cancer ; and to explore the central effect regulation mechanism of acupuncture intervention on hot flashes based on functional magnetic resonance imaging technology.

NCT ID: NCT05461248 Not yet recruiting - Rectal Cancer Clinical Trials

Stoma Discharge Reinfusion After Sphincter Preservation for Middle and Low Rectal Cancer

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

To analyze the occurrence of defecation complications, rectal function, and quality of life indicators after sphincter-preserving surgery for middle and low rectal cancer, the stoma exudate was collected before the stoma was restored, and the defecation complications, rectal function and quality of life indicators were evaluated. The effect of anal reinfusion of stoma discharge on the recovery of intestinal function in patients.

NCT ID: NCT05461534 Not yet recruiting - Breast Cancer Clinical Trials

Mindfulness Yoga and Sexual Functioning

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

Female breast cancer survivors with sexual dysfunction were randomly divided into a mindfulness yoga intervention group and a control group, and the investigators aimed to evaluate the effects of mindfulness yoga on sexual function in breast cancer survivors.

NCT ID: NCT05463471 Not yet recruiting - Shock Clinical Trials

Effect of Balanced Saline Solution and Albumin on Volume Expansion in Shock Patients

Start date: August 1, 2022
Phase: Phase 4
Study type: Interventional

To compare the direct effect of sodium acetate ringer injection or albumin on volume expansion in shock patients, and to provide reference for volume resuscitation strategy in shock patients

NCT ID: NCT05465733 Not yet recruiting - Non-Small-Cell Lung Clinical Trials

First-line Replacement Maintenance of Envafolimab in Advanced NSCLC

NSCLC
Start date: August 1, 2022
Phase: Phase 2
Study type: Interventional

This study is a single-center, prospective, single-arm phase II clinical study. For newly-treated patients with advanced NSCLC with negative driver gene and positive PD-L1 expression, those patients who did not progress after 4-6 cycles of PD-1 or PD-1 combined with chemotherapy standard treatment, after signing the informed consent form, were screened to meet the criteria for inclusion and exclusion. Standard, will receive Envafolimab combined with chemotherapy/Envafolimab single-agent first-line maintenance therapy until disease progression, withdrawal of informed consent, initiation of other anti-tumor therapy, death, or other protocol-specified conditions that should be discontinued Circumstances, whichever occurs first.

NCT ID: NCT05466045 Not yet recruiting - Uremic Pruritus Clinical Trials

Using of Extra Virgin Olive Oil in Hemodialysis Patients to Improve Pruritus and Sleep Disorders

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

Background and Purpose: Itching is a common complication of hemodialysis patients, which can cause skin damage and affect the patient's comfort. Studies have shown that olive oil is feasible and effective for pain relief, cancer treatment, stroke and cardiovascular disease, as well as wound healing and skin care because it is readily available, natural, and has merely no side effects, and there is no research application on the skin itchiness in hemodialysis patients. The purpose of this study was to investigate the effect of applying extra virgin olive oil to improve skin itching, sleep quality and changes in heart rate variability in hemodialysis patients. Research method: This study is designed as a randomized controlled trial (RCT), which is divided into two groups, the experimental group and the control group. Before the interventional measures, a questionnaire pre-test and HRV test are given first, and the interventional measures are given. During the period, in addition to routine care, both groups of patients used a brown roller ball glass bottle containing extra virgin olive oil or normal saline on the itchy skin every 12 hours gently and evenly smeared with fingers , for 28 days, and on the 14th day and 28 days.After intervention, the post-questionnaire test and HRV test were carried out. The research tools include: 5-D 5-D itch scale, Visual Analogue Scale (VAS), Pittsburgh Sleep Quality Index (PSQI) and Heart Rate Variability (HRV) detector.The data collection results were archived with Statistical Package for the Social Sciences (SPSS) statistical software, and the data were processed and analyzed by descriptive statistics, chi-square test, generalized estimating equation (GEE) and independent sample t test. Expected results: Result showed using extra virgin olive oil can improvement of skin itchiness and sleep quality in hemodialysis patients, and also cost effectiveness of lotions , reduction of drugs burden on kidneys and improvement of patients' quality of life.