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NCT ID: NCT05433402 Withdrawn - Clinical trials for Colon Cancer Stage III

Repurposing the Antipsychotic Drug Chlorpromazine as Adjuvant Therapeutic Agent for Resected Stage III Colon Cancer

Start date: July 20, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

chlorpromazine displays a series of remarkable bio-molecular effects in cancer cells, as inhibition of cell growth, nuclear aberrations, inhibition of the phosphoinositide 3-kinase/mammilian target of rapamycin (PI3K/mTOR) axis, induction of cytotoxic autophagy, inhibition of glutamate and DRD2 receptors. This study will evaluate the addition of chlorpromazine to the first-line therapeutic protocol in colon cancer stage III.

NCT ID: NCT04795596 Withdrawn - Ovarian Cancer Clinical Trials

Secondary Cytoreductive Surgery in Platinum-resistant Recurrent Ovarian Cancers

Start date: April 1, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This novel study was specifically designed for platinum resistant recurrent ovarian cancers and aimed to compare cases who received secondary cytoreductive surgery for isolated recurrence and chemotherapy versus chemotherapy alone. This comparison will conduct the intraoperative events, postoperative morbidity and mortality, pathological outcomes and long-term oncological outcomes as regarding progression free survival and overall survival rates.

NCT ID: NCT04738344 Withdrawn - Clinical trials for Coronary Artery Disease

Very Long Versus Overlapping Stents in Long Coronary Lesions

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

This study is performed to compare the angiographic and clinical outcomes of the use of single long stent versus overlapping stents in the treatment of long coronary lesions in patients with chronic coronary syndrome.

NCT ID: NCT04541719 Withdrawn - Labor Pain Clinical Trials

Patient Controlled Remifentanil Analgesia for Normal Labour

Start date: April 1, 2017
Phase: Phase 2
Study type: Interventional

Patient controlled remifentanil analgesia might offer comparative overall patient satisfaction and improved quality of analgesia after normal labour with continuous epidural analgesia.

NCT ID: NCT04532554 Withdrawn - Covid19 Clinical Trials

Growth Hormone in Obese Cases With Covid-19

Start date: October 26, 2020
Phase: Phase 4
Study type: Interventional

The use of growth hormone in obese cases with COVID-19 may help them to recover earlier.

NCT ID: NCT04434118 Withdrawn - Clinical trials for Rheumatoid Arthritis

Anti-rheumatic Drug Use and Risk of COVID-19 Infection in Rheumatoid Arthritis Patients

Start date: March 20, 2020
Phase:
Study type: Observational

Rheumatoid arthritis (RA) patients have an underlying immune deficiency and typically treated with immunosuppressive drugs, which may increase the risk of COVID-19 infection. Hydroxychloroquine (HCQ) has been found to possess antiviral activity against COVID-19. Thus, the aim of this study to investigate the ability of HCQ to reduce the risk of COVID-19 among RA patients.

NCT ID: NCT04433988 Withdrawn - COVID Clinical Trials

Efficacy of Pentoxifylline as Add on Therapy in COVID19 Patients

Start date: November 13, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

With potential antiviral effects on severe acute respiratory syndrome (SARS) and as a methyl-xanthine derived inhibitor of phosphodiesterase-4, pentoxifylline basically functions as a hemorrheologic agent for a better circulation and oxygenation and exerts unique effects on immune modulation, inflammation and oxidative stress. As the main regulator of cAMP metabolism, posphodiesterase-4 plays a key role in proinflammatory and immune cells. Pentoxifylline plays its anti-inflammatory role by reducing the production of proinflammatory cytokines such as TNF-a, IL-1 and IL-6. Given its unique impacts on immune modulation, homeostasis and fibrinolysis and its supportive effects on oxidative stress and organ failure, pentoxifylline can constitute a multipurpose and generally-safe adjuvant therapy for COVID-19 patients.

NCT ID: NCT04274803 Withdrawn - Clinical trials for Antiphospholipid Syndrome in Pregnancy

Dose Intralipid Infusion Reduces Pregnancy Complications Caused by Antiphospholipid Antibody Syndrome?

Start date: April 1, 2020
Phase: Phase 4
Study type: Interventional

This study will address the value of adding intralipid infusion in reducing pregnancy complications related to antiphospholipid syndrome

NCT ID: NCT04227730 Withdrawn - Clinical trials for Group B Streptococcal Infection

MATERNAL AND NEONATAL SCREENING FOR GROUP B STREPTOCOCCI : A Follow up STUDY

Start date: June 1, 2019
Phase:
Study type: Observational

Group B Streptococcus (GBS), is a facultative gram positive diplococcus originally known for causing bovine mastitis and was not demonstrated to be a human pathogen until 1938. In the 1970s, GBS emerged as the leading cause of neonatal morbidity and mortality, with a frequency of 2-3 cases per 1,000 live births and case-fatality ratios as high as 50%

NCT ID: NCT04193930 Withdrawn - ART Clinical Trials

Different Protocols in Ovarian Stimulation in Intracytoplasmic Sperm Injection Cycles

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

During assisted reproduction technology treatments like in vitro fertilization, some patients give a poor ovarian response to controlled ovarian hyperstimulation. The European Society of Human Reproduction and Embryology consensus defined poor response to ovarian stimulation during in vitro fertilization with Bologna criteria. Bologna criteria: At least two of the following three features must be present: (i) Advanced maternal age (≥40 years). (ii) Previous Poor responders (≤3 oocytes with a conventional stimulation protocol). (iii) An abnormal ovarian reserve test Most controlled ovarian hyperstimulation regimens currently used for expected poor responders are based on using a high daily dose (300- 450 IU/day) of exogenous gonadotropins. Giving a high gonadotropin dose obviously increases the cost of in vitro fertilization, a consequence that would be acceptable if paralleled by an improvement in in vitro fertilization outcome. Unfortunately, however, the available data suggest that increasing the daily gonadotropins dose may increase the number of retrieved oocytes, but not the final success rate of in vitro fertilization.