Stress Response Clinical Trials

11 recruitingLast updated: May 21, 2026

There are 11 actively recruiting stress response clinical trials across 7 countries. Studies span Not Applicable, Phase 4, Phase 1. Top locations include Alexandria, Alexandria Governorate, Egypt, Beverly Hills, California, United States, Chapel Hill, North Carolina, United States. Updated daily from ClinicalTrials.gov.


Stress Response Trials at a Glance

11 actively recruiting trials for stress response are listed on ClinicalTrialsFinder across 6 cities in 7 countries. The largest study group is Not Applicable with 7 trials, with the heaviest enrollment activity in Alexandria, Beverly Hills, and Chapel Hill. Lead sponsors running stress response studies include Tanta University, Central Institute of Mental Health, Mannheim, and Center for Advanced Facial Plastic Surgery.

Browse stress response trials by phase

About Stress Response Clinical Trials

Looking for clinical trials for Stress Response? There are currently 6 studies actively recruiting participants. Clinical trials offer access to new treatments before they are widely available, and every approved therapy in use today was first tested through a clinical trial.

Below you can browse trials, sign up for alerts when new Stress Response trials open, and view eligibility criteria for each study. Each listing includes the study phase, locations, and enrollment details.

Frequently Asked Questions

Common questions about Stress Response clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 111 of 11 trials

Recruiting
Not Applicable

CoreSys Monitoring for Intraoperative Stress Management in Abdominal Hysterectomy

surgical stress responseAnesthesiaInflammation+1 more
Hospital Provincial de Rosario30 enrolled1 locationNCT07571473
Recruiting
Phase 4

The Effect of Nocturnal Dexmedetomidine on Postoperative Sleep Quality and Fatigue After Major Surgery in Elderly Patients: DEXSLEEP Study

surgical stress responsePostoperative FatiguePostoperative Sleep Disturbances
Ziekenhuis Oost-Limburg102 enrolled1 locationNCT06480539
Recruiting
Not Applicable

Comparison of Stress Response Evoked by Conventional Versus Videolaryngoscope

Stress ResponseLaryngoscopyDuration
Sindh Institute of Urology and Transplantation124 enrolled1 locationNCT07510542
Recruiting
Not Applicable

Cranberry Polyphenols and Stress Resilience During Multitasking in Healthy Adults

Physiological StressMental StressMotor Activity+3 more
University of Florida84 enrolled1 locationNCT07453537
Recruiting
Not Applicable

Ultrasound Guided External Oblique and Rectus Abdominis Plane Block (EXORA) on Neuroendocrine Stress Response in Adults Undergoing Umbilical Hernia Surgery

Umbilical herniaUltrasoundExternal Oblique+2 more
Tanta University100 enrolled1 locationNCT07324863
Recruiting
Not Applicable

Do Increasing Preoperative Timing of Single Dexmedetomidine Dose Have an Effect on Stress Response of Laryngoscopy and Intubation?

DexmedetomidineIntubationStress Response+2 more
Tanta University45 enrolled1 locationNCT07165483
Recruiting
Not Applicable

Stress Trajectories and Anhedonia in Adolescence Research Study

AnhedoniaAdolescent DevelopmentStress Response
University of North Carolina, Chapel Hill192 enrolled1 locationNCT07040449
Recruiting
Phase 1

Impact of OnabotulinumtoxinA (BOTOX®) on Stress

StressStress (Psychology)Stress, Psychologic+4 more
Center for Advanced Facial Plastic Surgery20 enrolled1 locationNCT06778421
Recruiting
Not Applicable

Using Neurofeedback to Understand the Relationship Between Stress and Alcohol Consumption

Alcohol AbuseCravingPsychosocial Stressor+1 more
Central Institute of Mental Health, Mannheim102 enrolled1 locationNCT06247306
Recruiting
Phase 4

Effect of Dexmedetomidine Supplementation to General Anaesthesia in Paediatric Transcatheter Closure of Atrial Septal Defect

DexmedetomidineDelirium - PostoperativeAtrial Septal Defect (ASD)+1 more
Alexandria University30 enrolled1 locationNCT06631534
Recruiting

Yoga breathing and respiratory complications in surgical patients

surgical stress responsePostoperative pulmonary complications
Iva Pažur60 enrolled1 locationACTRN12622001312730