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Volumn 15, Issue 3, 1999, Pages 201-209
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Performance of the Frameless IUD (Flexigard prototype inserter) and the TCu380A after six years as part of a WHO multicenter randomized comparative clinical trial in parous women
a
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Author keywords
[No Author keywords available]
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Indexed keywords
COPPER INTRAUTERINE DEVICE;
ADULT;
ARTICLE;
BLEEDING;
CHINA;
CLINICAL TRIAL;
COMPARATIVE STUDY;
CONTRACEPTION;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
FEMALE;
FOLLOW UP;
HUMAN;
HUMAN EXPERIMENT;
INTERNATIONAL COOPERATION;
INTRAUTERINE CONTRACEPTIVE DEVICE;
MULTICENTER STUDY;
NORMAL HUMAN;
PAIN;
PATIENT ATTITUDE;
PERFORMANCE;
PREGNANCY RATE;
RANDOMIZED CONTROLLED TRIAL;
SAFETY;
TREATMENT FAILURE;
UTERUS CAVITY;
WORLD HEALTH ORGANIZATION;
ASIA;
CHINA;
CLINICAL RESEARCH;
COMPARATIVE STUDIES;
CONTRACEPTION;
CONTRACEPTIVE METHODS;
DEVELOPING COUNTRIES;
EASTERN ASIA;
FAMILY PLANNING;
IUD;
IUD, COPPER RELEASING;
LONGITUDINAL STUDIES;
RESEARCH METHODOLOGY;
RESEARCH REPORT;
STUDIES;
ADULT;
FEMALE;
HUMANS;
INTRAUTERINE DEVICE EXPULSION;
INTRAUTERINE DEVICES;
INTRAUTERINE DEVICES, COPPER;
PAIN;
PARITY;
PREGNANCY;
TIME FACTORS;
UTERINE HEMORRHAGE;
WORLD HEALTH ORGANIZATION;
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EID: 0033303808
PISSN: 02674874
EISSN: None
Source Type: Journal
DOI: 10.1023/A:1006797316253 Document Type: Article |
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Times cited : (8)
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References (11)
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