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حالة التجربة السريرية NCT07494877 لـ العقم هي يقبل مشاركين. اطلعوا على جميع التفاصيل في عرض البطاقة الخاص برادار التجارب السريرية وأدوات اكتشاف الذكاء الاصطناعي. أو يمكنكم طرح أي سؤال هنا.
تجربة واحدة تطابق معايير الفلتر
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Effect of Anticoagulant Therapy on Endometrial Receptivity and Pregnancy Outcomes in Infertility ٣٠٠ رصدية

يقبل مشاركين
تفاصيل التجربة السريرية متاحة بشكل أساسي باللغة الإنجليزية. ومع ذلك، يمكن لـ رادار التجارب AI مساعدتك؛ ما عليك سوى النقر على «وصف الدراسة» لعرض ومناقشة معلومات التجربة باللغة التي اخترتها.
التجربة السريرية NCT07494877 هي دراسة رصدية لـالعقم وهي يقبل مشاركين. بدأت في ٩ ربيع الأول ١٤٤٧ هـ مع خطة لتجنيد ٣٠٠ مشاركًا. يقودها Tang-Du Hospital، ومن المتوقع اكتمالها بحلول ٣ شعبان ١٤٤٩ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٨ شوال ١٤٤٧ هـ.
الملخص
The purpose of this prospective observational cohort study is to evaluate the effect of routine clinical anticoagulant therapy on endometrial receptivity and subsequent pregnancy outcomes in women with infertility. Researchers will utilize an ultrasound multimodal system to systematically assess endometrial parameters, including thickness, morphology, peristalsis, and blood flow indices. The study aims to enroll appr...عرض المزيد
وصف مفصل
Background and Rationale:

Endometrial receptivity plays a pivotal role in the success of embryo implantation for patients with infertility. Impaired endometrial perfusion is considered a significant contributing factor to implantation failure. In routine clinical practice, anticoagulant therapies, such as low-dose aspirin and low molecular weight heparin (e.g., heparin sodium), are frequently utilized to improve loc...

عرض المزيد
العنوان الرسمي

Evaluation of the Effect of Anticoagulant Therapy on Endometrial Receptivity and Pregnancy Outcomes in Patients With Infertility Using an Ultrasound Multimodal System

الحالات الطبية
العقم
معرّفات دراسة أخرى
  • K202508-28
NCT معرّف
تاريخ البدء (فعلي)
2025-09-01
آخر تحديث مُنشور
2026-03-27
تاريخ الاكتمال (المقدر)
2027-12-31
عدد المشاركين المخطط لهم
٣٠٠
نوع الدراسة
رصدية
الحالة
يقبل مشاركين
الكلمات الرئيسية
Endometrial Receptivity
Anticoagulant Therapy
Multimodal Ultrasound
مجموعات/التدخلات
مجموعة المشاركين/الذراعالتدخل/العلاج
Anticoagulant Therapy Cohort
Patients in this cohort receive routine clinical anticoagulant therapies (such as low-dose aspirin or low molecular weight heparin) in addition to their conventional infertility treatment. The use of anticoagulants is determined by the attending physician based on standard clinical indications, strictly independent of this observational study protocol.
Routine Anticoagulant Therapy (Aspirin or Heparin Sodium)
Patients receive low-dose aspirin or low molecular weight heparin (e.g., heparin sodium) purely as part of their standard clinical care. The decision to initiate, adjust, or terminate this therapy is made entirely by the attending physician based on clinical indications, strictly independent of this observational study protocol. This is tracked solely as an observational exposure.
Conventional Treatment Cohort
Patients in this cohort receive conventional infertility treatment only, without the addition of anticoagulant therapies, as per standard clinical practice.
غ/م
النتيجة الرئيسية
مقياس النتيجةوصف القياسالإطار الزمني
Clinical Pregnancy Rate
The clinical pregnancy rate is defined as the proportion of patients with the presence of at least one intrauterine gestational sac with a visible fetal heartbeat, confirmed by transvaginal ultrasound.
Up to 90 days of gestation
النتيجة الثانوية
مقياس النتيجةوصف القياسالإطار الزمني
Endometrial Thickness
The maximum anteroposterior diameter of the endometrium measured in millimeters (mm) in the midsagittal plane using 2D transvaginal ultrasound.
During the window of implantation (prior to embryo transfer)
Endometrial Morphological Pattern
Evaluated via 2D transvaginal ultrasound and classified into three typical patterns: Type A (triple-line pattern), Type B (intermediate isoechogenic pattern), and Type C (homogeneous hyperechogenic pattern) to assess morphological receptivity.
During the window of implantation (prior to embryo transfer)
Endometrial and Subendometrial Blood Flow Indices
Quantitative assessment of local tissue perfusion using 3D power Doppler ultrasound. The parameters measured include Vascularization Index (VI, reflecting vessel density), Flow Index (FI, reflecting blood flow intensity), and Vascularization Flow Index (VFI, a combination of vascularity and flow intensity).
During the window of implantation (prior to embryo transfer)
Endometrial Peristalsis Frequency
The frequency of endometrial wave-like activity (contractions per minute) observed via continuous transvaginal ultrasound scanning for a duration of 3 to 5 minutes.
During the window of implantation (prior to embryo transfer)
Early Miscarriage Rate
The proportion of patients who experience a spontaneous pregnancy loss after the initial ultrasound confirmation of an intrauterine clinical pregnancy, prior to 90 days of gestation.
Up to 90 days of gestation
مساعد المشاركة
معايير الأهلية

الأعمار المؤهلة للدراسة
بالغ
العمر الأدنى للدراسة
20 Years
الجنس المؤهل
أنثى
  • Female patients aged 20 to 45 years.

Clinically diagnosed with infertility and planning to undergo embryo transfer or monitored conception cycles.

Patients who have complete baseline clinical data and are willing to undergo multimodal ultrasound evaluation of endometrial receptivity during the window of implantation.

Voluntarily agreed to participate in this observational study and signed the informed consent form for data collection.

  • Presence of congenital uterine malformations (e.g., septate uterus, bicornuate uterus, unicornuate uterus) that significantly alter the endometrial cavity.

Presence of untreated severe intrauterine lesions, such as submucosal fibroids, severe intrauterine adhesions, or endometrial polyps that may mechanically interfere with implantation.

Severe underlying systemic diseases, including but not limited to severe liver or kidney dysfunction, or malignant tumors.

Known severe bleeding disorders or strict contraindications to anticoagulant medications (for patients in the routine clinical care setting).

Patients who are unable to cooperate with the transvaginal multimodal ultrasound examination or complete the required follow-up for pregnancy outcomes.

Tang-Du Hospital logoTang-Du Hospital
الجهة المسؤولة عن الدراسة
zhangli, المحقق الرئيسي, Associate Chief Physician, Tang-Du Hospital
جهة اتصال مركزية للدراسة
جهة اتصال: Li Zhang, MD, 86-29-84778860, [email protected]
جهة اتصال: Zhengjun Ma, MM, +86-13072977233, [email protected]
1 مواقع الدراسة في 1 بلدان

Shaanxi

Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, 710038, China
Li Zhang, MM, جهة اتصال, 86-29-84778860, [email protected]
Zhengjun Ma, MM, جهة اتصال, +86-13072977233, [email protected]
يقبل مشاركين