PTSD Trial, Recruiting NCT07204535 Sponsor: Centre Paul Strauss Condition: PTSD
Back to Ptsd

PTSD Trial, Recruiting

NCT07204535
Recruiting Not Applicable

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:

  • You have been diagnosed with cervical cancer and your doctors have recommended a specific type of internal radiation treatment called brachytherapy (high-dose rate or pulse-dose rate)
  • Your cervical cancer can be of any cell type, including squamous cell carcinoma or others
  • You are generally able to carry out daily activities, with at most some limitations (your doctor will assess this using a standard health scale)
  • You are able to read and complete questionnaires written in French
  • You are willing to give your consent to take part in the study
  • You are 18 years old or older

Who may not be able to join:

  • You have difficulty understanding or answering questionnaires because of a cognitive condition, a learning disability, a language barrier, or a mental health condition that affects your judgment
  • You are currently under a legal protection order (for example, if someone else is legally responsible for making decisions on your behalf)
  • You are currently pregnant or breastfeeding

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: George NOEL, MD, PhD, ICANS, CPS

Phone: 368767223

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Centre Paul Strauss
Registry
ClinicalTrials.gov
Start date
17 November 2025
Est. completion
17 November 2030

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Post-Traumatic Stress Disorder evaluation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov