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NCT ID: NCT03995004 Suspended - Effect of Drugs Clinical Trials

The Effect of Melatonin on Postoperative Pain Reduction After Orthognathic Surgery

Start date: October 2022
Phase: Phase 1
Study type: Interventional

Orthognathic surgery is a procedure performed to correct dentofacial deformities. It involves osteotomy at the facial skeleton. Considerable pain is expected in the early recovery period. Melatonin is a hormone that is produced naturally by the body. Synthetic Melatonin is available over the counter for the management of sleeping disorder and jetlag. Clinically, Melatonin can also be used to reduce pain and analgesic consumption in patients undergoing surgery. Dexamethasone is a type of steroid. It can suppress the inflammatory response. It is an anti-inflammatory, anti-allergic drug. It is commonly used in head and neck and oral surgery for its anti-inflammatory effect to reduce swelling. This study aims evaluate the efficacy of oral melatonin in the pain reduction following orthognathic surgery. This is a double-blinded randomized controlled trial. We will recruit 87 patients who are scheduled for double-jaw orthognathic surgery to participate in this three-year study. The study lasts for 2 weeks. Participant will be randomly allocated by computer to one of the three groups. (1) Group D will receive dexamethasone only; (2) Group M will receive melatonin only; and (3) Group DM both melatonin and dexamethasone. Postoperative pain level and perioperative plasma levels of inflammatory markers and anti-oxidizing enzymes will be recorded and compared among the study groups.

NCT ID: NCT03791372 Recruiting - Safety Issues Clinical Trials

Clinical Effect and Safety of Autologous Umbilical Cord Blood Transfusion in the Treatment of Cerebral Palsy

Start date: October 10, 2017
Phase: Phase 1
Study type: Interventional

To study the clinical efficacy and safety of autologous umbilical cord blood transfusion in the treatment of cerebral palsy.

NCT ID: NCT03760900 Completed - Safety Issues Clinical Trials

Safety of Autologous Cord Blood Cells for Preterm Infants.

Start date: January 1, 2009
Phase: Early Phase 1
Study type: Interventional

To assess the safety of autologous volume- and red blood cell (RBC)-reduced non-cryopreserved umbilical cord blood (UCB) cell infusion to preterm infants.

NCT ID: NCT03700177 Recruiting - Anesthesia, Local Clinical Trials

Ropivacaine 0,2% Plus Dexamethasone Versus Ropivacaine 0,2% Plus Placebo in Modified Pectoral Block

Start date: February 1, 2019
Phase: Phase 4
Study type: Interventional

To find out if dexamethasone used as adjuvant to ropivacaine, a long-lasting local anesthetic, prolongs the duration of modified pectoral nerve block in women undergoing breast surgery.

NCT ID: NCT03696745 Not yet recruiting - Safety Issues Clinical Trials

The Treatment of Premature Infants With Brain Injury by Autologous Umbilical Cord Blood Stem Cells

Start date: November 1, 2018
Phase: Phase 1
Study type: Interventional

To study the safety and effect of autologous umbilical cord blood stem cells for treatment brain injury

NCT ID: NCT03683953 Not yet recruiting - Safety Issues Clinical Trials

The Treatment of Bronchopulmonary Dysplasia by Intratracheal Instillation of Mesenchymal Stem Cells

Start date: September 29, 2018
Phase: Phase 1
Study type: Interventional

To study the effect and saftey of intratracheal instillation of mesenchymal stem cells for treatment BPD

NCT ID: NCT03600506 Not yet recruiting - Effect of Drugs Clinical Trials

Dexmedetomidine Adjuvant to General Anesthesia of Abdominal Hysterectomy

Start date: August 2018
Phase: N/A
Study type: Interventional

To assess the effect of perioperative Dexmedetomidine infusion on Interleukin 6 and cortisol level in patients undergoing general anesthesia for total abdominal hysterectomy

NCT ID: NCT03488186 Completed - Safety Issues Clinical Trials

PK-PD Comparative Study of Lansoprazole Capsules and Lansoprazole Enteric-coated Capsules in Healthy Chinese Volunteers

Start date: July 19, 2018
Phase: Phase 1
Study type: Interventional

The objective of this study was to compare the relative PK-PD of Lansoprazole Capsules and Lansoprazole DR Capsules in healthy Chinese volunteers.

NCT ID: NCT03488173 Completed - Safety Issues Clinical Trials

Pharmacokinetic Study of Lansoprazole Capsules in Healthy Chinese Volunteer

Start date: April 23, 2018
Phase: Phase 1
Study type: Interventional

The objective of this study was to compare pharmacokinetic of Lansoprazole Capsules 30 mg with Lansoprazole Capsules of Takeda 30 mg in healthy adult human subjects.

NCT ID: NCT03339882 Completed - Safety Issues Clinical Trials

Remifemin Preventing the Climacteric Symptoms in Breast Cancer

Start date: January 4, 2017
Phase: Phase 2
Study type: Interventional

LHRH-a is an important hormone treatment in breast cancer especially in high-risk hormone receptor-positive patients or hormone receptor-negative but needing ovarian function protecting. The climacteric symptoms caused by LHRH-a are often and prominent, which is a common clinical problem.