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CTRI Number  CTRI/2019/01/016919 [Registered on: 04/01/2019] Trial Registered Prospectively
Last Modified On: 12/05/2022
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study
Modification(s)  
Drug
Other (Specify) [endometrial sampling]  
Study Design  Randomized, Parallel Group, Multiple Arm Trial 
Public Title of Study   Understanding reasons behind fewer pregnancies in Indian women suffering from endometriosis and adenomyosis; and finding appropriate treatment to improve it 
Scientific Title of Study   Understanding molecular mechanism of Implantation Failure in Women with Endometriosis and Adenomyosis Undergoing In-vitro Fertilization and Methods to Improve their Fertility Outcomes 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Sunita Sharma 
Designation  MD, FNB 
Affiliation  Institute of Reproductive Medicine 
Address  Department of ART Institute of Reproductive Medicine HB/36/A/3, sector III Salt lake, Kolkata

Kolkata
WEST BENGAL
700106
India 
Phone  03323215125  
Fax    
Email  sunitapalchaudhuri@yahoo.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Baidyanath Chakravarty 
Designation  MD FNB 
Affiliation  Institute of Reproductive Medicine 
Address  Department of ART Institute Of Reproductive Medicine HB/36/A/3 sector III Salt lake, Kolkata

Kolkata
WEST BENGAL
700106
India 
Phone  03323215125  
Fax    
Email  bncirm@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Sunita Sharma 
Designation  MD FNB 
Affiliation  Institute of Reproductive Medicine 
Address  Department of ART Institute of Reproductive Medicine, HB/36/A/3 sector III Salt lake, Kolkata

Kolkata
WEST BENGAL
700106
India 
Phone  03323215125  
Fax    
Email  sunitapalchaudhuri@yahoo.com  
 
Source of Monetary or Material Support  
Institute Of Reproductive Medicine 
 
Primary Sponsor  
Name  Institute Of Reproductive Medicine 
Address  HB/36/A/3 sector III Salt lake 
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr BN Chakravarty  Institute of Reproductive Medicine  Department of ART Institute of Reproductive Medicine HB 36/A/3 Sector III Salt Lake, Kolkata 700106
Kolkata
WEST BENGAL 
03323215125

bncirm@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTE ETHICS COMMITTEE INSTITUTE OF REPRODUCTIVE MEDICINE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: N972||Female infertility of uterine origin, (2) ICD-10 Condition: N972||Female infertility of uterine origin, (3) ICD-10 Condition: N719||Inflammatory disease of uterus, unspecified,  
 
Intervention / Comparator Agent
Modification(s)  
Type  Name  Details 
Comparator Agent  GnRH agonist  Patients will be injected depot preparation of 3.75 mg of GnRH-agonist every 28 days for 3 months. Sonographic features of adenomyosis will be assessed before and after 3 months of treatment. Patients will be subjected to endometrial sampling before and after therapy. Markers such as aromatase enzyme, alpha V Beta 3 integrin Estrogen alpha and beta receptor etc. will be assessed. IVF outcome parameters will be assessed. 
Intervention  Letrozole  Patients will be given oral dose of Letrozole 2.5 mg thrice weekly for 3 months. Sonographic features of adenomyosis will be assessed before and after 3 months of treatment. Patients will be subjected to endometrial sampling before and after intervention. Markers such as aromatase enzyme, alpha V Beta 3 integrin Estrogen alpha and beta receptor etc. will be assessed. IVF outcome parameters will be assessed. 
 
Inclusion Criteria  
Age From  25.00 Year(s)
Age To  39.00 Year(s)
Gender  Female 
Details  Women with Grade III and Grade IV endometriosis and adenomyosis of 25-40 years with regular menstrual cycles (25-32 days), euthyroid with normal baseline hormone levels will be included.  
 
ExclusionCriteria 
Details  Women with stage I and II endometriosis, fibroids, hydrosalpinx, uterine size >12 weeks, uterine abnormalities, follicle stimulating hormone (FSH) >12 IU/ml, polycystic ovary syndrome, any pelvic pathology including pelvic inflammatory disease and adhesions and male factor infertility will be excluded 
 
Method of Generating Random Sequence
Modification(s)  
Computer generated randomization 
Method of Concealment
Modification(s)  
On-site computer system 
Blinding/Masking
Modification(s)  
Outcome Assessor Blinded 
Primary Outcome
Modification(s)  
Outcome  TimePoints 
A. To evaluate VAS and PBAC of patients suffering from symptomatic adenomyosis with or without endometriosis, before and after the treatment.
B. To evaluate and compare the Live birth following different treatment strategies.
C. To evaluate the molecular markers of implantation in these patients and compare them with controls, before and after treatments.
1. Aromatase Enzyme
2. Estrogen receptor-alpha and beta receptor
3. Progesterone Receptor
4. VEGF
5. eNOS
 
VAS & PBAC: May 2022 - May 2023
Molecular Marker Assessment: June 2022 - June 2023
Live Birth : June 2023 - May 2024
 
 
Secondary Outcome
Modification(s)  
Outcome  TimePoints 
A. To evaluate the sonographic features of adenomyosis, before and after treatment.
B. To evaluate and compare biochemical pregnancy rate, clinical pregnancy rate and miscarriage rate.  
Sonographic Feature assessments: May 2022 - June 2023

Reproductive outcome: September 2022 - September 2023 
 
Target Sample Size   Total Sample Size="210"
Sample Size from India="210" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)
Modification(s)  
16/05/2022 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial
Modification(s)  
Years="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details
Modification(s)  
Sharma S, Bathwal S, Agarwal N, Chattopadhyay R, Saha I, Chakravarty B.; Does presence of adenomyosis affect reproductive outcome in IVF cycles? A retrospective analysis of 973 patients. Reprod Biomed Online. 2018: S1472-6483(18)30518-2. 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Brief Summary
Modification(s)  

Adenomyosis is an uterine pathology characterized by the invasion of endometrial glands and stroma in the myometrium leading to disruption of uterine junctional zone. Women with adenomyosis usually have symptoms of progressive dysmenorrhoea and menorrhagia though some cases may be asymptomatic1. It is found in a high proportion of infertile (24.4%) patients especially in those with endometriosis, repeated miscarriage and recurrent implantation failure and in older women seeking in-vitro fertilization (IVF) treatment2.

The dysmenorrhoea associated with adenomyosis as well as endometriosis may sometimes be so debilitating that the pain management takes precedence over fertility treatment. Medical management of pain associated with these disease processes takes longer time and thus losing the precious years of reproductive age. The evidence showing effect of adenomyosis and endometriosis in assisted reproductive technologies (ART) outcome is controversial3,4. Some researchers have reported decreased implantation rate and negative reproductive outcomes with adenomyosis; however, others failed to observe such association. Although various mechanisms have been postulated regarding the impact of adenomyosis on infertile women, the underlying molecular events responsible for implantation failure in these women remains unclear.

The increased expression of P450 aromatase has been observed in women with endometriosis and adenomyosis5. It is reported that endometrial aromatase expression has been associated with poor reproductive outcomes in IVF6. One of the actions of Letrozole and GnRH agonist is the suppression of endometrial aromatase expression. Few studies have reported that long term use of GnRH agonists before IVF treatment has improved reproductive outcome. The effect of Letrozole on the treatment of adenomyosis before IVF treatment is yet to be studied.  

Review of literature:

 Endometriosis and adenomyosis is an estrogen-dependent disorder and is associated with increased aromatase expression5. It has been reported that in infertile women the prevalence of adenomyosis with endometriosis is estimated as 79% and without endometriosis as 28%7. The impact of adenomyosis on natural conception or fertility treatment is not clear. The proposed mechanisms responsible for infertility and poor reproductive outcome in adenomyosis may be abnormal junctional zone  myometrium leading to dysregulation of uterotubal contractility8, altered endometrial function and receptivity and abnormal decidualization8 Cytokines, prostaglandins and other inflammatory mediators lead to excessive free radical formation which may deteriorate oocyte quality and embryo development in adenomyosis9. It is hypothesized that free radicals lead to activation of macrophages and T cells and also increased nitric oxide exposure resulting in early miscarriage10.

 Kitawaki et al. demonstrated the expression of P450 aromatase protein and mRNA in adenomyotic tissue and eutopic endometrium of adenomyosis, but it was not detected in the endometrium of women without adenomyosis. It is reported that increased endometrial aromatase expression is associated with poor reproductive outcomes in IVF5  

Letrozole has been used as a medical treatment for endometriosis associated pain11 and might improve the IVF success rates in a subset of women with endometriosis12. Use of Letrozole inhibits aberrant expression of aromatase in endometriosis and balances estrogen and progesterone action. It normalize the ability of progesterone to down-regulate estrogen receptors, which is essential during implantation.13

 GnRH agonist, mainly used in endometriosis for pain management, has also been found to decrease expression of P450arom in the eutopic endometrium of women with adenomyosis and endometriosis.13 A 3-month hormonal therapy before IVF might therefore create a more favorable environment for oocyte maturation, with better oocyte quality and better fertilization rates as well as embryo quality. However the longer duration of stimulation and the higher amount of medication needed argue against this treatment.

Aim of our study is to evaluate molecular marker of implantation in women with adenomyosis and endometriosis, and to assess the role and compare letrozole and GnRH agonist in improving implantation and reproductive outcome in these women undergoing IVF.

 

Objectives:

1. To assess and compare the reduction in dysmenorrhea/menorrhagia and sonographic features of adenomyosis in Indian women.


2. To evaluate the molecular markers of implantation in patients with adenomyosis alone or with endometriosis and compare them with controls.


3. To evaluate and compare different treatment approaches from molecular perspectives to improve the implantation failure.


4. 
To further assess and compare the post-treatment implantation and reproductive outcome for the proposed treatment approaches in adenomyosis undergoing in vitro fertilization.

 
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