Clinical trials: Time Management
Wounds
Study of the Efficacy of Sharp Debridement for the Management of Chronic Wounds
Standard care of care and up to twelve (12) weekly debridements. Subjects randomized into the weekly debridement group will receive up to twelve (12) debridement during the twelve (12) weeks of the study.
- Trial name
- NCT00990522
- Testing
- debridement
- Sponsor
- Southwest Regional Wound Care Center
Conscious Sedation
Post-Marketing Clinical Study to Assess Efficacy and Safety of Dexmedetomidine in Post-Operative Patients
The purpose of this study is to assess efficacy and safety of dexmedetomidine at the time of extubation and after extubation, in patients requiring postoperative sedation in the ICU.
- Trial name
- NCT00318955
- Testing
- Dexmedetomidine, Propofol
- Where
- 13 sites in Japan
- Volunteers
- 85 people
- Sponsor
- Hospira, now a wholly owned subsidiary of Pfizer
Unexplained Infertility
Dual FSH/HCG Trigger in Letrozole Stimulated Intrauterine Insemination Cycles in Women With Unexplained Infertility
The objective of this study was to evaluate the outcome of follicle stimulating hormone (FSH) co-administration with human chorionic gonadotrophins trigger for women with unexplained infertility (UEI) and assigned for letrozole…
- Trial name
- NCT02739516
- Testing
- Human chorionic gonadotropin, FSH co-trigger, Letrozole
- Volunteers
- 108 people
- Sponsor
- Benha University
Respiratory Aspiration
Acceptability and Feasibility of a New Postural Management Night-time Intervention to Improve Respiratory Health of Children With Complex Neuro-disability
This research concerns children with complex neuro-disability. Damage to the developing brain leads to lifelong disturbances in motor control, seizures, cognition, communication, eating and drinking, and behaviour.
- Trial name
- Breathe-Easy (NCT06039852)
- Testing
- Novel Postural Management Night-time Intervention
- Where
- United Kingdom
- Volunteers
- 10 people
- Sponsor
- Sussex Community NHS Foundation Trust
Healthy
A Study in Healthy Subjects to Investigate Whether Administration of Lucerastat Can Affect Normal Heart Function
Two-part Phase 1 study to assess the effect of single therapeutic and supra-therapeutic doses of lucerastat on the QT/QTc interval duration in healthy subjects (Part A: Pilot study; Part B: TQT study)
- Trial name
- NCT03832452
- Testing
- Lucerastat (Treatment A), Moxifloxacin, Lucerastat (Treatment B)
- Where
- Netherlands
- Volunteers
- 44 people, healthy volunteers welcome
- Sponsor
- Idorsia Pharmaceuticals Ltd.
Endometriosis
A Multinational, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Investigate the Efficacy, Safety and Duration of Effect of a Single Administration of Various Doses of Cetrorelix SR in Subjects With Histologically Confirmed Endometriosis
Identify effective doses of cetrorelix SR in the treatment of symptoms of endometriosis, describe dose effect relationship and duration of symptom relief
- Trial name
- NCT00244452
- Testing
- Cetrorelix
- Where
- 57 sites in Australia, Belgium and 6 more
- Sponsor
- Solvay Pharmaceuticals
Solid Tumor, Metastatic Bone Disease
Evaluate Time Associated With the Preparation & Administration of Denosumab/Pamidronate in Patients With Solid Tumors and Metastatic Bone Disease
This study will estimate the total time for the preparation and administration of denosumab and the total time for the preparation and administration of pamidronate.
- Trial name
- NCT02101164
- Testing
- denosumab, pamidronate
- Sponsor
- Amgen
Follicular Tonsillitis (Chronic)
Effect of Intravenous Fentanyl on the Occurrence of Postoperative Nausea and Vomiting According to Time of Administration Around the End of Tonsillectomy With or Without Adenoidectomy
Fentanyl is a commonly used drug for the prevention of emergence agitation and reduction in postoperative pain in children receiving tonsillectomy.
- Trial name
- NCT03343002
- Testing
- fentanyl at 10-15 min before end of surgery, fentanyl at end of surgery
- Where
- South Korea
- Volunteers
- 140 people
- Sponsor
- Yonsei University
the Hemodynamic Parameters, Intubation Times
The Use of Airtraq Laryngoscope Versus Macintosh Laryngoscope and Fiberoptic Bronchoscope by Experienced Anesthesiologists
The investigators hypothesize that when used by experienced anesthesiologists, Airtraq laryngoscope will increase the first-attempt success rate with shorter intubation times and more stable hemodynamic parameters.
- Conditions
- the Hemodynamic Parameters, Intubation Times, Complications During and After Intubation
- Trial name
- NCT01917565
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Marmara University
In-vitro Fertilization
Time-lapse Evaluation of Human Embryo Development in Single Versus Sequential Culture Media - a Sibling Oocyte Study
Current human IVF technology employs two strategies with respective culture media for embryo development; 'let the embryo choose' (utilizes single step media) and 'back-to-nature' (utilizes sequential media).
- Trial name
- NCT01507883
- Where
- Turkey (Türkiye)
- Volunteers
- 50 people
- Sponsor
- Bahceci Health Group
Asthma Management, Time Restricted Eating
Investigating the Impact of Early Time-Restricted Eating on Health Outcomes and Quality of Life in Adults With Mild Controlled Asthma Compared to Healthy Adults
This study aims to explore how early time-restricted eating (eTRE) - where all daily meals are eaten within a specific time window - affects health and quality of life in adults.
- Trial name
- eTRE (NCT07345572)
- Testing
- Early Time-Restricted Eating (eTRE) and Habitual Diet (HD), Habitual Diet (HD) and Early Time-Restricted Eating (eTRE)
- Where
- United Kingdom
- Volunteers
- 36 people
- Sponsor
- De Montfort University
Polyp of Colon, Colorectal Polyp
Artificial Intelligence Development for Colorectal Polyp Diagnosis
Accurate classification of growths in the large bowel (polyps) identified during colonoscopy is imperative to inform the risk of colorectal cancer.
- Trial name
- NCT06447012
- Testing
- Colonoscopy
- Where
- United Kingdom
- Volunteers
- 4,000 people
- Sponsor
- King's College Hospital NHS Trust
Diabetes Mellitus, Type 2, Time Restricted Feeding
Time-Restricted Eating for Type II Diabetes: TRE-T2D
This is a randomized clinical trial to assess the feasibility and efficacy of time-restricted eating (TRE) to improve glucose regulation and cardiovascular health of participants with type 2 diabetes mellitus (T2DM).
- Conditions
- Diabetes Mellitus, Type 2, Time Restricted Feeding, Diabetes type2
- Trial name
- TRE-T2D (NCT05365529)
- Testing
- Time-Restricted Eating, Standard of Care
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of California, San Diego
Liver Diseases
Fibrinogen Concentrates Versus Cryoprecipitate in Liver Transplant Surgery
We compared the time consumed for goal-directed management of hypofibrinogemia using two strategies during liver transplant (LT) surgery: a conventional cryoprecipitate-based strategy versus a lyophilized fibrinogen…
- Trial name
- NCT06144112
- Testing
- fresh frozen plasma, prothrombin complex concentrate
- Where
- South Korea
- Volunteers
- 92 people, healthy volunteers welcome
- Sponsor
- Konkuk University Medical Center
Papilloma Virus, Human
IMPAACT P1085: Human Papilloma Virus (HPV) Type-Specific Antibody
This study is being done to evaluate how long the immune response from the Human Papilloma Virus (HPV) vaccine you / your child received persists.
- Trial name
- HPV (NCT01206556)
- Where
- 23 sites in United States, Puerto Rico
- Volunteers
- 97 people
- Sponsor
- International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Spinal Anesthesia, Postoperative Pain Management
Intravenous Dexamethasone for Prolonging Sensory Block in Spinal Anesthesia
The goal of this clinical trial is to learn if intravenous dexamethasone can help prolong the effect of spinal anesthesia in adults having elective pelvic, urologic, or proctologic surgery.
- Conditions
- Spinal Anesthesia, Postoperative Pain Management, Dexamethasone, Pelvic Surgery
- Trial name
- NCT07088432
- Testing
- Dexamethasone
- Where
- Tunisia
- Volunteers
- 120 people
- Sponsor
- Tunis University
Spinal Anesthesia, Cesarean Section
The Role of Carotid Flow Time-Based Fluid Administration in Caesarean Section
It has been reported that corrected carotid flow time (FTc) may indicate the responsiveness of spontaneously breathing patients to fluid therapy.
- Trial name
- NCT06048497
- Testing
- Corrected carotid flow time measurement guided fluid preload
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 72 people
- Sponsor
- Cukurova University
Migraine Disorders
Management of Migraine Using Enerumab and Traditional Therapy at the Time of COVID-19
The objective of this study was to assess the efficacy of erenumab on frequency of monthly migraine days in adults at baseline, 3 months and 6 months, disability in patients with chronic migraine and on post covid migraine…
- Trial name
- NCT05052008
- Testing
- Erenumab
- Where
- Egypt
- Volunteers
- 90 people
- Sponsor
- Fayoum University
Myocardial Perfusion Imaging
Real-Time Myocardial Perfusion Echocardiography in the ICU
This study is being done to find out if and how much the use of RTMPE improves a provider's confidence in the diagnosis they assign.
- Trial name
- NCT03173716
- Testing
- Definity
- Where
- United States
- Volunteers
- 24 people
- Sponsor
- Mayo Clinic
Recurrent Low Back Pain
B Vitamin Supplementation to Chiropractic Management of Chronic LBP: Pilot Clinical Trial (VCLBP)
The purpose of this investigation is to assess the effects of a combination of B vitamins (B6 [pyridoxine],, B9 [folate], and B12 [cyanocobalamin] upon the efficacy and duration of spinal manipulation in its treatment of chronic…
- Trial name
- VCLBP (NCT06576739)
- Testing
- Spinal Manipulation
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of Western States