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EndometriosisPhase 2LET-DAN RCTNCT07183787

Letrozole vs Danazol for Endometriosis-Related Pain: Randomized Trial

A Phase 2 study testing Letrozole and danazol in people with Endometriosis, run by Sidra Salman at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background: Endometriosis is a chronic gynecological condition defined by the ectopic presence of endometrial glands and stroma outside the uterine cavity, most commonly diagnosed via laparoscopy. While its exact etiology remains uncertain, a positive family history is considered a significant risk factor. Read more about this study

Who is it for?
Ages 18 to 45 years, women only
Conditions the study is for
Endometriosis
What is being tested?
Letrozole and danazol
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 sitePakistan
Study dates
10 Apr 2019to 31 Jul 2025
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Women aged 18-45 years
  • Surgically or clinically diagnosed endometriosis
  • Moderate to severe pelvic pain (NRS ≥ 4 for at least 3 months)
  • Willing to use effective contraception during the study
  • Able to provide informed consent

Who cannot join

  • Pregnant or breastfeeding
  • Severe hepatic disease, thromboembolic disorder, or contraindication to study drugs
  • Use of hormonal therapy within the last 8 weeks
  • Known hypersensitivity to Letrozole or Danazol
  • Participation in another clinical trial within the last 3 months

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Sharif Medical and Dental College

    Lahore, Punjab Province, 54700

Other trials in Pakistan

About this study

Official title: Comparison of Letrozole Versus Danazole for Pain Management of Female Presenting With Endometriosis

Background:

Endometriosis is a chronic gynecological condition defined by the ectopic presence of endometrial glands and stroma outside the uterine cavity, most commonly diagnosed via laparoscopy. While its exact etiology remains uncertain, a positive family history is considered a significant risk factor. Danazol has historically demonstrated efficacy in alleviating endometriosis-related pain, while letrozole, primarily used in neoadjuvant settings, has recently emerged as a promising alternative. This study aimed to compare the mean reduction in pain scores between letrozole and danazol in women with laparoscopically confirmed endometriosis.

Read more

Objective:

To compare the efficacy of letrozole versus danazol in reducing pain scores among women diagnosed with endometriosis.

Material \& Methods:

Study Design: Randomized control trial Setting: Department of Obstetrics \& Gynaecology, Sharif Medical and Dental Hospital

Read the detailed description

Introduction:

Endometriosis is defined by the ectopic presence of functional endometrial glands and stroma outside the uterine cavity, most commonly diagnosed via direct laparoscopic visualization (1). Clinical manifestations include dysmenorrhea, dyspareunia, chronic pelvic pain, and infertility-each of which may significantly impair a woman's quality of life (2). It is a chronic, estrogen-dependent inflammatory condition predominantly affecting women of reproductive age, though adolescents may also be affected (3). Its true prevalence remains uncertain due to underdiagnosis and a diagnostic delay averaging nearly a decade, often attributed to normalization of symptoms and missed recognition by primary care providers. Beyond physical symptoms, endometriosis exerts a profound psychosocial and economic burden on affected individuals, their families, and healthcare systems globally (4).

Pathophysiology and Clinical Impact of Ectopic Endometrial Tissue in Endometriosis Ectopic endometrial tissue typically localizes in the dependent regions of the pelvis, such as the posterior and anterior cul-de-sac, uterosacral ligaments, ovaries, and fallopian tubes; however, extra-pelvic involvement is also possible (5). These implants respond to cyclic hormonal stimulation much like eutopic endometrium, undergoing phases of proliferation, secretion, and subsequent shedding. The metabolic by-products especially cytokines and prostaglandins foster a chronic inflammatory milieu characterized by neovascularization, fibrosis, and pain sensitization. Immunologic dysregulation is also implicated, including aberrant T- and B-cell responses, complement system activation, and elevated interleukin-6 (IL-6) levels in affected individuals. These immunoinflammatory mechanisms lead to adhesion formation, anatomic distortion, and chronic pelvic pain which are the hallmark features of the disease (5).

Classification of Endometriosis:

Endometriosis can be classified into three main types based on lesion location. Superficial peritoneal endometriosis is the most common form, characterized by lesions affecting the peritoneum, the thin membrane lining the pelvic cavity. Endometriomas, or ovarian lesions, are dark, fluid-filled cysts ("chocolate cysts") that develop within the ovaries, often resistant to treatment and capable of damaging healthy ovarian tissue. Deeply infiltrating endometriosis extends beneath the peritoneal surface and may involve adjacent pelvic organs such as the bowel or bladder, occurring in approximately 1% to 5% of affected women (6). (Figure 1).

Figure 1: An Illustration that is an overview of the three primary types of endometrioses based on lesion location: superficial peritoneal lesions, ovarian endometriomas, and deeply infiltrating endometriosis.

Comparative Evaluation of Letrozole and Danazol for Pain Reduction in Females with Endometriosis

Despite varied symptoms, endometriosis diagnosis is often delayed due to the absence of reliable non-invasive biomarkers. Current hormone therapies and analgesics offer limited long-term efficacy, as recurrence is common. Letrozole, an aromatase inhibitor, competitively binds to the cytochrome P450 subunit, reducing estrogen biosynthesis and offering a novel approach to managing endometriosis (7). Letrozole, an aromatase inhibitor, has demonstrated effectiveness in reducing endometriosis-related pain without recurrence post-treatment (8). Danazol, a synthetic androgen, suppresses ovarian activity and modulates immune function but has shown inconsistent results in pain management across studies (9). Although hormone therapies such as letrozole and danazol are widely used for symptom management, existing literature reports conflicting evidence regarding their effectiveness in reducing endometriosis-related pain. The present study seeks to answer the research question: "Among females diagnosed with endometriosis, how does the reduction in pain scores with letrozole therapy compare to danazol therapy over a three-month period, and which agent offers more consistent and sustained pain relief to inform standardized treatment protocols?" Addressing this question may improve patient outcomes in management of pain. So, this study aims to compare letrozole with danazol's impact on pain reduction in females with endometriosis, to guide future treatment protocols and update local clinical guidelines.

Conditions
Endometriosis
Being tested
Letrozole, danazol
Medical subject headings
Endometriosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LetrozoleDrug

    Letrozole 2.5 mg orally once daily for 12 weeks.

  • danazolDrug

    Danazol 200 mg orally twice daily for 12 weeks.

Study groups in NCT07183787
Study groupRoleWhat they receive
Arm 1: LetrozoleExperimentalParticipants in this arm will receive Letrozole 2.5 mg orally once daily for 12 weeks for management of endometriosis-related pelvic pain.
Receives: Drug: Letrozole
Arm 2: DanazolActive comparatorParticipants in this arm will receive Danazol 200 mg orally twice daily for 12 weeks for management of endometriosis-related pelvic pain.
Receives: Drug: danazol

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in pelvic pain severity (0-10 Numeric Rating Scale)

    Mean change in pelvic pain scores measured on a 0-10 numeric rating scale; lower scores indicate improvement.

    Measured: 12 weeks

Secondary outcomes (1)
  1. Change in dysmenorrhea severity

    Change in dysmenorrhea severity recorded on a standardized 0-10 numeric rating scale; lower scores indicate improvement.

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Sep 2025
  2. Study start10 Apr 2019
  3. Primary completion10 Oct 2019
  4. Study completion31 Jul 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Model description
This is a randomized, parallel-group trial with two treatment arms. Participants will be allocated to receive either Letrozole or Danazol for management of endometriosis-related pain. Each participant will remain in their assigned arm throughout the study period.
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07183787
Sponsor's protocol ID
SMDC/SMRC/79-18
Acronym
LET-DAN RCT
Status last verified
Dec 2019
First submitted
14 Sep 2025
Last updated
19 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Haqnawaz F, Virk S, Qadir T, Imam S, Rizvi J. Comparison of Letrozole and Clomiphene Citrate Efficacy along with Gonadotrophins in Controlled Ovarian Hyperstimulation for Intrauterine Insemination Cycles. J Reprod Infertil. 2013 Jul;14(3):138-42.

    PubMed 24163798
  • García E, Cruz OP. Regulation of Inflammation Pathways and Inflammasome by Sex Steroid. Reproduction and the Inflammatory Response. 2022:607539061.

  • Khashchenko EP, Uvarova EV, Fatkhudinov TK, Chuprynin VD, Asaturova AV, Kulabukhova EA, Vysokikh MY, Allakhverdieva EZ, Alekseeva MN, Adamyan LV, Sukhikh GT. Endometriosis in Adolescents: Diagnostics, Clinical and Laparoscopic Features. J Clin Med. 2023 Feb 20;12(4):1678. doi: 10.3390/jcm12041678.

    PubMed 36836214
  • Arafah M, Rashid S, Akhtar M. Endometriosis: A Comprehensive Review. Adv Anat Pathol. 2021 Jan;28(1):30-43. doi: 10.1097/PAP.0000000000000288.

    PubMed 33044230
  • Rasul SG, Yaqub U, Manzoor M, Mubasshar H. Comparison of Letrozole versus Danazol for the pain management of females presented with endometriosis. Annals of King Edward Medical University. 2017;23(4):514-8.

  • Mehmud G, Akhtar T, Sadia S. Endometriosis: frequency and correlation between symptomatology and disease stage. J Coll Physicians Surg Pak. 2007 Apr;17(4):199-202.

    PubMed 17462175

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Letrozole and danazol in people with Endometriosis, run by Sidra Salman at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in pelvic pain severity (0-10 Numeric Rating Scale) (time frame: 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07183787, which also lists 6 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Sep 2025; AzTrials last refreshed its copy on 7 Nov 2026.

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