Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT07419594

Estradiol and Intrusive Memories

Led by Charite University, Berlin, Germany · Updated on 2026-02-19

273

Participants Needed

1

Research Sites

184 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the current project is to investigate the impact of 3mg of oral estradiol valerate on the formation of intrusive memories after analog trauma. A well-established stress-film paradigm will be used to induce intrusive symptoms in healthy participants. In a double-blind placebo-controlled study, the impact of oral estradiol on intrusive symptoms during and immediately after exposure to a trauma film will be examined. The primary hypothesis is that exogenous oral estradiol will decrease the number of intrusive memories recorded in the four days following experimental trauma compared with placebo controls. This project will contribute to the current understanding of intrusive memory formation in PTSD and may guide the development of future pharmacological preventions.

CONDITIONS

Official Title

Estradiol and Intrusive Memories

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy female volunteers
  • German language proficiency at B1 level
  • Age between 18 and 45 years
Not Eligible

You will not qualify if you...

  • Current or past mental disorder diagnosed by DSM-5
  • Any physical illness
  • Taking any medication except oral contraceptives
  • History of traumatic experiences such as sexual abuse or rape
  • Pregnancy or breastfeeding
  • Use of oral contraceptives
  • Currently in the follicular phase of the menstrual cycle

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Charité - Universitätsmedizin Berlin

Berlin, State of Berlin, Germany, 12203

Actively Recruiting

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Research Team

T

Tolou Maslahati, M.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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