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Not yet recruitingNCT07821320Updated Sep 18, 2026

Impact of the Antihistamine Desloratadine on the Quality of Life and Dysmenorrhea in Patients With Endometriosis

A Phase 2 interventional study of Desloratadine and Placebo in Endometriosis, Endometriosis (Diagnosis) and Endometriosis and Dysmenorrhea, sponsored by Medical University of Vienna. Not yet recruiting at 1 site in Austria. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by Medical University of Vienna · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

Endometriosis is a chronic inflammatory disease affecting approximately 10% of women in their reproductive years. It is characterized by the presence of endometrial-like tissue outside the uterine cavity. Current treatment options include hormonal therapies or surgical excision of the endometriotic lesions. Although these interventions often lead to a significant symptom relief, some patients still experience persistent pain or treatment-related adverse effects. Consequently, the management of dysmenorrhea and improvement of quality of life in patients with endometriosis remain a clinical challenge.

Desloratadine is widely used for the treatment of allergic rhinitis or chronic urticaria. Recent studies suggest that desloratadine may also possess analgesic and anti-inflammatory properties. So far, however, no clinical studies have investigated its potential therapeutic effects in patients with endometriosis.

Therefore, the present study aims to provide the first clinical assessment of the efficacy, safety and tolerability of desloratadine in patients with endometriosis.

02

Conditions studied

  • Endometriosis
  • Endometriosis (Diagnosis)
  • Endometriosis and Dysmenorrhea
  • Endometriosis Associated Pelvic Pain
03

In context

Endometriosis

920 studies on the registry are indexed under Endometriosis; 266 are open to participants now.

This study's planned enrollment of 60 is below the median of 67 across 540 interventional studies indexed under Endometriosis.

Browse Endometriosis studies →

Lead sponsor

Medical University of Vienna is the lead sponsor of 1,109 studies on the registry; 184 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female patients aged 18-50
  • By imaging (sonography or MRI) or surgery last 10 years confirmed endometriosis
  • EHP-30 Score > 40

Exclusion criteria

Exclusion Criteria:

  • Subject is unable or unwilling to participate
  • History of malignant diseases
  • Current treatment
  • History of allergies and/or usage of antihistaminic treatments
  • women
  • Current hormonal treatment
  • Surgical treatment \<1year
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Placebo comparator
    Control-Group

    Drug: Placebo

  • Active comparator
    Drug-Group

    Drug: Desloratadine

Interventions

06

What researchers measure

Primary outcomes

  1. Change in the Endometriosis-Health-Profile-30 (EHP-30) Score

    The Score is used to measure the impact of Endometriosis on the quality of life. It is standardised on a scale from 0 to 100. 0 indicates the best health status whereas 100 indicates the worst health status.

    Time frame: from enrollment to the end of treatment at 150 days"

Secondary outcomes

  1. Change in Dysmenorrhea using the visual analogue scale (0-10)

    Time frame: From enrollment to the end of treatment at 150 days

07

Study locations

1 site
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07821320
Responsible party
René Wenzl (Ao. Univ.-Prof. Dr. med. univ. René Wenzl, MSc, Medical University of Vienna) — Principal investigator
First posted
Sep 15, 2026
Start date
Feb 2027 (estimated)
Primary completion
Feb 2028 (estimated)
Completion
May 2028 (estimated)
Last update
Sep 18, 2026

Study contacts

Marina Stjepic
Contact
marina.stjepic@meduniwien.ac.at
+431404065190

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Desloratadine

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