Effect of Drug

9

Review clinical trials related to Effect of Drug. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Efficacy and Safety of Remimazolam Besylate for Sedation in Post-Non-Cardiac Surgery Patients Requiring Mechanical Ventilation

A multi-center, prospective, randomized, double-blind, active-controlled, no-inferiority clinical trial conducted across 5 tertiary medical centers in China. The objective of this RCT is to evaluate the sedative efficacy and safety profile of remimazolam besylate compared with dexmedetomidine in patients requiring mechanical ventilation following non-cardiac surgery. The study hypothesized that remimazolam besylate is non-inferior to dexmedetomidine regarding the primary efficacy outcome.

Participants needed: 306
Trial details
Phase: Phase 4Age: 18-64Biological sex: AllType: InterventionalSponsor: Beijing Shijitan Hospital, Capital Medical UniversityUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Aged between 18 and 64 years [+6]

Undergoing intracranial surgery, or having a history of severe neurological or s... [+10]

Status: Recruiting

Effects of Salbutamol in Athletes and Implications for Screening and Sports

β2-Agonists, commonly used to treat asthma, have also been used by athletes to enhance performance, leading to their ban by the International Olympic Committee in 1972. Research has shown non-asthmatics receive no benefit from these drugs at therapeutic dosages; however, many elite athletes still use them, and asthmatic athletes often win more Olympic medals. In some non-asthmatics, β2-agonists may improve breathing limitations during high intensity exercise, which may improve performance. Therefore, we aim to examine if there is a select group of non-asthmatic individuals who experience breathing limitations that may receive benefit from β2-agonists.

Participants needed: 64
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Aerobic capacity (V̇O2max) greater than 120% predicted [+3]

Smoking history or currently smoking. Currently smoking is defined as regular us... [+5]

Status: Recruiting

Compare the Efficacy and Outcome Between Fentanyl and Morphine as Analgo-sedation in Mechanically Ventilated Patients

The primary aim of this clinical trial is to compare the effectiveness of fentanyl vs morphine as analgosedation in mechanically ventilated adult patients in the ICU. This study also aims to compare the outcomes of patients between the two groups. The main questions it aims to answer are : 1. Does propofol and fentanyl infusion as analgo-sedation achieve targeted sedation score at 12 and 24 hours compared to propofol and morphine infusion in mechanically ventilated adult patients in the intensive care unit (ICU)? 2. Is there a difference between the proportion of patients requiring rescue sedation dose between the fentanyl and morphine groups?

Participants needed: 116
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Universiti Sains MalaysiaUpdated: Oct 6, 2025Locations: 1
Eligibility criteria

Age >18 years old [+2]

Patients with chronic use of narcotics [+7]

Status: Recruiting

Efficacy of Solifenacin or Mirabegron With Local Estrogen Versus Combination Pharmacotherapy for Overactive Bladder

To investigates the effects of solifenacin or mirabegron with local estrogen versus combination treatment with solifenacin and mirabegron in women with overactive bladder

Participants needed: 300
Trial details
Phase: Phase 4Age: 40-90Biological sex: FemaleType: InterventionalSponsor: Mackay Memorial HospitalUpdated: May 9, 2025Locations: 1
Eligibility criteria

Patients with detrusor overactivity which defined as a urodynamic observation ch...

Postvoid urine retention before treatment [+2]

Status: Recruiting

Efficacy of Combined Pharmacotherapy Versus Solifenacin With Vaginal Estrogen Cream for Women With Detrusor Overactivity

To investigates the effects of combined pharmacotherapy with solifenacin and mirabegron versus solifenacin with vaginal estrogen cream in women with detrusor overactivity.

Participants needed: 200
Trial details
Phase: Phase 4Age: 40-90Biological sex: FemaleType: InterventionalSponsor: Mackay Memorial HospitalUpdated: May 9, 2025Locations: 1
Eligibility criteria

Patients with detrusor overactivity which defined as a urodynamic observation ch...

Postvoid urine retention before treatment [+3]

Status: Recruiting

Evaluation the Efficacy Between Botox Injection and Combination Pharmacotherapy in Patients With Detrusor Overactivity

To investigates the effects of botulinum toxin type A bladder injection compared to combined pharmacotherapy with Mirabegron and Solifenacin.

Participants needed: 300
Trial details
Phase: Phase 4Age: 20-90Biological sex: FemaleType: InterventionalSponsor: Mackay Memorial HospitalUpdated: May 9, 2025Locations: 1
Eligibility criteria

Patients with detrusor overactivity which defined as a urodynamic observation ch...

Postvoid urine retention before treatment

Status: Not yet recruiting

Efficacy of Biological Therapy in Pediatric Inflammatory Bowel Disease

Compare efficacy of different biologicals in induction of remission including clinical, laboratory and histopathological remission.

Participants needed: 40
Trial details
Phase: Early Phase 1Age: 1-16Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Dec 19, 2024
Eligibility criteria

Not listed

Status: Recruiting

Comparing Trypsin-Chymotrypsin and Naproxen Sodium for Post-endodontic Treatment Pain

This study aims to compare the pain reduction efficacy of Trypsin-Chymotrypsin and Naproxen sodium after root canal treatment in patients with symptomatic irreversible pulpitis. A lot of patients suffer greatly from post endodontic treatment pain and have a fear of dental treatments due to the pain. Patients refuse to go to the dentists and neglect oral hygiene care. That's why it is very important to find an effective drug regimen to reduce this post treatment pain. The null hypothesis is that there will be no difference between the efficacy and mean pain scores of Trypsin-chymotrypsin and Naproxen Sodium for post-endodontic treatment pain. Conducted as a triple-blinded, parallel, randomized controlled trial, 100 patients will be randomly assigned to receive either Trypsin-Chymotrypsin or Naproxen sodium following standard root canal therapy. Pain levels will be assessed using a numerical rating scale at 1, 6, 12, and 24 hours post-treatment to evaluate the effectiveness of these two pain management modalities.

Participants needed: 100
Trial details
Phase: Phase 4Age: 18-45Biological sex: AllType: InterventionalSponsor: Dow University of Health SciencesUpdated: Nov 4, 2024Locations: 1
Eligibility criteria

Both male and female, healthy patients (ASA class 1). [+3]

Patients who will require emergency dental treatment. [+5]

Status: Recruiting

Effect of Captopril on GLS in Duchenne Myodystrophy

To outline the intermediate term effect of prescribing Captopril as an add on therapy on Left ventricular functions as measured by Global longitudinal strain in patients with Duchenne myodystrophy (DMD)

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 6+Biological sex: MaleType: InterventionalSponsor: Ain Shams UniversityUpdated: Jul 16, 2024Locations: 1
Eligibility criteria

Genetically confirmed Duchenne myodystrophy (DMD) patients with abnormal GLS < -...

Any patient who refuses to sign an informed consent. [+2]