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NCT ID: NCT05606796 Recruiting - Effect of Drug Clinical Trials

Comparison of Preserved and Preservative-free Latanoprost 0.005% in Primary Open Angle Glaucoma and Ocular Hypertensive Patients, at Guinness Eye Centre, Lagos.

Start date: December 2022
Phase: Phase 4
Study type: Interventional

It is a randomised, double-blinded clinical trial in which consenting participants who meet the inclusion criteria would be randomised into 2 groups. Subjects will be given either preserved or preservative free latanoprost for a period of 12 weeks. The efficacy and tolerability of both drugs would be assessed every 4 weeks, amongst these patients.

NCT ID: NCT05596721 Not yet recruiting - Asthma Clinical Trials

Azithromycin Treatment for Non-eosinophilic Chest Tightness Variant Asthma

Start date: January 1, 2023
Phase: Phase 4
Study type: Interventional

Bronchial asthma (abbr. asthma) is one of common airway chronic inflammatory disease which usually threatens human health. Typical symptoms of asthma are recurrent wheezing, shortness of breath, chest tightness and cough, usually happened at night or in early morning. However, there are still some patients who persist only clinical manifestations of chest tightness, namely, chest tightness variant asthma (CTVA). This subgroup of asthma usually lacks asthma-specific clinical features, therefore, often misdiagnosed and lack of effective treatment for a long time. The investigators' previous studies have found that CTVA has eosinophilic and non-eosinophilic subtypes. These patients with non-eosinophilic CTVA (NE-CTVA) are not sensitive to ICS/LABA, which guidelines recommend. At present, the specific treatment plan for NE-CTVA is urgently needed to elucidate. Azithromycin has immunomodulatory and anti-inflammatory effects in addition to their antibacterial effects. Maintenance treatment with azithromycin has been proved to be effective in chronic neutrophilic airway diseases and severe asthma. However, there are no clinical studies to confirm the effectiveness of azithromycin in non-eosinophilic asthma, especially atypical asthma such as NE-CTVA. Now the investigators performed a national multi-center study to explore whether azithromycin improves asthma symptom control and improves quality of life in people with NE-CTVA. Finally, to find an optimal treatment for NE-CTVA.

NCT ID: NCT05595044 Recruiting - Effect of Drug Clinical Trials

Effect of Vitamin D Therapy in Autism Spectrum Disorder

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

The aim of this work is to study the adjuvant effect of vitamin D supplementation on inflammatory marker (IL4) and habilitation outcome in children with Autism Spectrum Disorder in order to evaluate its efficiency as a treatment option based on correction of immune dysfunction.

NCT ID: NCT05543304 Enrolling by invitation - Effect of Drug Clinical Trials

Predicting Response to Systemic Therapies for Hepatocellular Carcinoma(HCC)

Start date: December 1, 2018
Phase:
Study type: Observational

As the most common type of primary liver cancer, hepatocellular carcinoma (HCC) has become a big challenge all over the world. Most patients are not available to curative resection when first diagnosed. There are a variety of treatment options for advanced HCC. However, due to the heterogeneity of HCC, the overall response rate (ORR) is not high for systemic therapies. Therefore, appropriate selection of patients who are suitable for individual systemic therapies is important for clinical decision-making.

NCT ID: NCT05510986 Not yet recruiting - Effect of Drug Clinical Trials

The Effect of Oxycodone Hydrochloride on CRBD After TURBT Under General Anesthesia

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

The purpose of this study is to investigate the effect of Oxycodone Hydrochloride on catheter-related bladder discomfort in patients undergoing transurethral resection of bladder tumor after general anesthesia.

NCT ID: NCT05482451 Recruiting - Effect of Drug Clinical Trials

Nivolumab and All-trans Retinoic Acid for Pancreatic Cancer

Start date: March 1, 2021
Phase: Early Phase 1
Study type: Interventional

This study is to examine the anticancer activity of the combination therapy with all-trans retinoic acid and nivolumab in patients with chemotherapy-refractory advanced or metastatic pancreatic adenocarcinoma.

NCT ID: NCT05479747 Completed - Effect of Drug Clinical Trials

Efficacy of Trypsin-Chymotrypsin On Post-operative Pain After Single Visit Root Canal Treatment

Start date: June 1, 2021
Phase: Phase 4
Study type: Interventional

Achieving effective pain control after endodontic treatment is still a disruptive event to all the clinicians. There is a knowledge gap regarding the effect of protease on postoperative pain following root canal treatment, therefore, the efficacy of Trypsin-Chymotrypsin on post endodontic pain was evaluated clinically in a randomized triple-blind trial.

NCT ID: NCT05456113 Enrolling by invitation - Effect of Drug Clinical Trials

Topical Cannabidiol Application and Skin Vascular Reactivity

cannabidiol
Start date: December 1, 2024
Phase: N/A
Study type: Interventional

Cannabidiol, or CBD, is an over-the-counter "nutraceutical" that is more commonly being used by healthy adults for pain management, recovery from strenuous exercise, and general wellness. However, little research exists on the effects of CBD in otherwise healthy individuals. This study uses iontophoresis, a common technique used in physical therapy, to determine the effectiveness of topical CBD in lessening the reflex increased cutaneous vascular conductance response to stimulation of the skin.

NCT ID: NCT05438979 Recruiting - Effect of Drug Clinical Trials

Joint Health Study

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

Natural dietary health supplements that may improve quality of life by relieving joint discomfort have been of increasing interest. Recent studies have demonstrated promising effects of one such supplement - calcium fructoborate (CFB). Preliminary evidence suggests that CFB may reduce joint discomfort, however, few well-powered studies have been conducted to assess the true effects of this supplement. In this study, conducted virtually, we will examine changes in joint discomfort over a 90 day period. Participants will be randomized to receive either 216mg CFB or placebo (i.e., 216mg microcellulose) to take every day for the study period.

NCT ID: NCT05401825 Recruiting - Effect of Drug Clinical Trials

Antenatal COVID 19 Vaccination and Pregnancy Outcomes

Start date: February 18, 2022
Phase:
Study type: Observational

Effect of COVID 19 vaccinations on pregnancy outcomes must be clear and identified to detect their safty