Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:13 AM
Ignite Modification Date:
2025-12-25 @ 2:13 AM
NCT ID:
NCT01509560
Eligibility Criteria:
Inclusion Criteria:
* Patients after allogeneic stem cell transplantation aged ≥ 18 years
* Prophylaxes of GvHD with calcineurin inhibitors (Ciclosporine A, Tacrolimus) and MTX or MMF (previous therapy of acute GvHD with additional prednisone is permitted)
* Increased risk of chronic GvHD, defined by
* Male with female donor
* HLA mismatch class I- or II towards GvHD
* Persistant active acute GvHD on day +50 after stem cell transplantation despite of high-dose steroids and cyclosporine
* Reduction of baseline FEV1 or DLCO (examined 0 - 50 days before transplantation) of ≥ 25%
* New occurrence of acute GvHD between day +50 and +100 after stem cell transplantation
* Informed concent
Exclusion Criteria:
* Use (prophylactic or therapeutic) of mTor inhibitors after SCT
* Overlap of acute and chronic GvHD
* Total cholesterol ≥ 3-fold of upper limit (UL) or triglycerides ≥ 3-fold UL
* GOT, GPT, Bilirubin ≥ 3-fold UL (if not related to GvHD)
* Creatinine ≥ 3-fold UL
* Confirmed active hepatitis B or C
* All circumstances where impaired wound healing might be a risk factor, esp. surgical interventions in the last weeks, ulcers of skin or mucosa
* Known intolerance to Everolimus, Sirolimus or other compoments of Certican®
* Lactose intolerance
* Pregnancy or lactation
* Women in reproductive age, except of women with the following criteria:
* Postmenopausal (12 month natural amenorrhea)
* Postoperativ (≥ 6 months after bilateral ovariectomy with / without hysterectomy)
* During therapy and at least 6 months after the last application of Everolimus: regular and correct high-effective contraception (Pearl-Index \< 1; e. g. oral contraception, intrauterine device, implantate, contraceptive patch, combination of barrier methods (condom and cervical cap/diaphragm), abstinence
* Men, not using one of the following methods of contraception during therapy and at least 6 month after the last application of Everolimus:
* Sexual abstinence
* Vasectomy
* Condom
* Impairments or diseases reducing the ability of informed consent
* Participation of another study (e.g. for prophylactic immunsuppression in the stem cell transplantation procedure) within the last 60 day before recruitment
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01509560
Study Brief:
Protocol Section:
NCT01509560