Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults between 18 and 65 years old who are scheduled for a planned (non-emergency) keyhole gallbladder removal surgery
- People who have been assessed by an anaesthetist as generally healthy or having only mild health conditions (this is known as ASA class I or II)
- People who are able to understand what the study involves and are willing to sign a consent form
- People who have healthy, intact skin at the areas where the electrode pads would be placed for the treatment
- People who are willing to complete pain, anxiety, and satisfaction rating scales before and after surgery
Who may not be able to join:
- People who have been assessed as having moderate to severe health conditions by an anaesthetist (ASA class III or higher)
- People who have a cardiac pacemaker or any other electrical device implanted in their body
- People with a history of epilepsy, severe nerve damage, or a psychiatric condition that affects how they experience pain or anxiety
- People who have skin wounds, infections, or skin conditions in the areas where the electrode pads would need to be placed
- People who are taking pain relief, anti-anxiety, or sedative medications beyond what is normally given as part of standard surgical care
- People whose surgery becomes an emergency procedure or whose keyhole surgery needs to be converted to open surgery during the procedure
- Women who are pregnant or breastfeeding
- People who are unwilling or unable to sign a consent form
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +90, 0543 805 62 09
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Postoperative Pain Intensity (VAS); Postoperative Pain Intensity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.