Peritoneal Carcinomatosis Clinical Trial
— Hypericin-PDTOfficial title:
Pilot Study on Intra-abdominal Photodynamic Diagnosis in Peritoneal Carcinosis
The study would examine by hypericin-supported Fluoreszenzlaparoskopy in terms of tumor size, number and location of the combination of photodynamic diagnosis (PDD) and therapy (PDT) with regard to the detection of peritoneal metastases of locally advanced gastric cancer at 50 adult patients.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | July 2020 |
Est. primary completion date | December 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - = 18 years - Computertomography - morphologically locally - advanced gastric cancer (Classification of Malignant Tumours (TNM): size or direct extent of the primary tumor > 3 or degree of spread to regional lymph nodes positive) without distant metastases (except peritoneum) - Histologically confirmed adenocarcinoma of the stomach - Karnofsky Index > 70 Exclusion Criteria: - Patients who are considered inoperable because of a reduced general condition: - Congestive heart failure (New York Heart Association (NYHA) Functional Classification III / IV), - Severe coronary heart disease, non-treatable arrhythmia or non-adjustable hypertension, - Severe asthma suffering (Chronic obstructive pulmonary disease) - Distant metastases except peritoneum - Patients with a contraindication related to the present study - Allergy or intolerance to the study drug or a substance with chemical similarity to the study medication. - Lack of capacity to consent - Participation in another interventional therapy studies at intervals of 30 days - Contraindication to taking the prescribed study medication the physician's discretion - Pregnancy/ Breastfeeding - Women in childbearing age who refuse: - Simultaneously apply two appropriate contraceptive measures or maintain a full hetero-sexual abstinence at least 28 days prior to the study and for at least 28 days after administration of study medication - To stop breast-feeding during the study and through 6 months after the end of study - Men who refuse: - To use a latex condom during any sexual contact with childbearing women during the study and at least 28 days after completion of study, even if they are successful vasectomy. - - Sperm donor to make up at least 28 days after completion of study.- |
Country | Name | City | State |
---|---|---|---|
Germany | University Department of General, Visceral and Transplant Surgery | Tübingen | Baden.Württemberg |
Lead Sponsor | Collaborator |
---|---|
University Hospital Tuebingen |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Peritoneal metastases in terms of tumor size [centimeter, cm] | Detection of peritoneal metastases of locally - advanced gastric cancer by hypericin - supported Fluoreszenzlaparoskopie in terms of tumor size [cm] | Day 1 (day of surgery) | |
Primary | Peritoneal metastases in terms of number [n] | Detection of peritoneal metastases of locally - advanced gastric cancer by hypericin - supported Fluoreszenzlaparoskopie in terms of number [n] | Day 1 (day of surgery) | |
Primary | Peritoneal metastases in terms of location | Detection of peritoneal metastases of locally - advanced gastric cancer by hypericin - supported Fluoreszenzlaparoskopie in terms of location [central, right upper, epigastrium, left upper, , left flank, left lower, pelvis, riht lower, right flank, upper jejunum, lower jejunum, upper ileum, lower illeum] | Day 1 (day of surgery) | |
Secondary | Hypericin level | Hypericin levels in the peritoneum and serum the day of surgery | Day 1 (day of surgery) | |
Secondary | Histological evidence of apoptosis | Histological evidence of apoptosis in peritoneal metastasis after photodynamic therapy | Day 1 (day of surgery) |
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