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Ic venlafaxine hcl er 37.5 mg, ethinyl estradiol 100 µg, and levonorgestrel 5 µg. Study Design and Methods Patient Selection and Population Patients were recruited from a national random sample of patients who had an IUD inserted between May 1993 and January 1996. Inclusion criteria for this study were: at or before the visit when counseling was started, had not previously received an IUD, and agreed to proceed with the counseling Venlafaxine 90 Pills 2mg $285 - $3.17 Per pill if indicated. Of eligible patients, 1,973 (83.6%) were enrolled by June 1996. Patients were excluded if they had a previous expulsion (n = 5), required emergency contraception (N = 2), required vasectomy 1), had a history of Buy atorvastatin pelvic infection (such as Chlamydia trachomatis or trichomoniasis) (n = 1), a previous ectopic pregnancy (n = 2), or if the patient was less than 16 years of age (n = 1). Study Interventions and Interrater Reliable Confidence Intervals Couples met with study staff 3 weeks before the counseling session to review study regimen. The couples were asked if they would be willing to participate in the study and to state whether they would like to be randomized receive a levonorgestrel-releasing intrauterine system (LNG-IUS), copper-containing copper IUD (IUDC), or a levonorgestrel-releasing copper T-380A IUS. The study team met with couple again 2 weeks before enrollment to review the IUDC instructions with couple if they had not already received the instructions. study team gave couple a packet and them letter to return the clinic. study team explained that all information had been kept confidential and the information was being made available to the patient and clinic. letter explained that the IUDC was intended to be placed in the uterus 3 weeks after IUD placement and that the copper-containing IUD was intended to be placed within 3 weeks after the IUD placement. letter also explained that a return visit with the study team was planned within two weeks to review the patient's history and assess any unintended pregnancies. The study started week of IUD placement when the family of an eligible woman received the study packet and letter. clinic provided counseling sessions from 3 to 5 h per week, depending on the woman's cycle. counseling sessions were conducted by a female staff member who was trained to conduct the sessions. physician who provided counseling was trained to administer study medications at the recommended dosages and to provide support of the patient as recommended by and her family. During each counseling session, the staff gave patients a printout of detailed instructions and the patient did not need to attend sessions. Interrater Reliable Confidence Interval Both study staff and patients were asked to record whether study medication was administered correctly or not during follow-up visits. The clinic personnel recorded these assessments. The study staff had access to information from all of the study patients for first 36 months of the study to confirm accuracy of the data. A second trained physician from the study staff provided a final assessment 6 months after the end of study to confirm and update the data. In addition to physician's final assessment, a third study nurse provided an 8-wk period of supervised supervision to the research associates (see Methods section for details). Patient's Self-Reported History To determine the frequency of IUD use in the women enrolled study, study were asked to report.
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