Schedule of Visits Sample Clauses

Schedule of Visits. Table 1 describes the broad outline of the schedule of visits provided for in the Scheme. Number of Weeks of Pregnancy Visit to General Practitioner Visit to Chosen Maternity Unit/Hospital Before 12 weeks (preferably as soon as possible after conception) * Before 20 weeks * 24 * 28 * (Except in case of first pregnancy) * (In case of first pregnancy) 30 * 32 * 34 * 36 * 37 * 38 * 39 * 40 * Birth of the Baby 2 Weeks after birth (for baby) * 6 Weeks after birth (for mother and baby) * This schedule may be changed by either the general practitioner or obstetrician, for example where the patient suffers from a major condition (e.g. diabetes/ hypertension) which requires special care. However, care in respect of illnesses which are coincidental with but not related to the pregnancy does not form part of the Scheme. After the birth of the baby, the public health nurse will visit mother and baby in their home to give advice and support. (The mother may, if she so wishes be contacted by the Public Health Nurse during pregnancy).
Sample 1
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Schedule of Visits. A schedule of study activities by visit is shown in Appendix 1. A detailed list of activities conducted at each study visit is also described in the following section. VISIT 1: Screening: · Obtain written informed consent; · Obtain medical history; · Assess xxxxx xxxxx, weight, height, waist circumference, and BMI; · Administer ***, and ***; · Assess inclusion/exclusion criteria; · Obtain blood and urine samples for laboratory analyses, and perform urine pregnancy test (female subjects of childbearing potential only); · Schedule a follow-up visit in 2 weeks (±1 week). VISIT 2: Randomization: Week 0: · Perform urine pregnancy test (female subjects of childbearing potential only); · Perform physical examination including ECG evaluation (can be done at any time between screening; · If screening laboratory results and physical examination findings are acceptable, obtain randomization assignment through IVRS; · Assess weight, waist circumference, and xxxxx xxxxx; · Administer *** for *** and ***, and perform *** (see Section 7.4); · Perform 24-hour dietary recall with subject and review lifestyle modifications; · Dispense assigned titration kit and provide instructions for proper use; · Assess adverse events (including eye pain), and changes in concomitant medications; · Schedule next follow-up visit in 2 weeks (±2 days). VISIT 3: Titration: Week 2: · Perform urine pregnancy test (female subjects of childbearing potential only); · Assess weight, waist circumference, and xxxxx xxxxx; · Administer *** and ***; · Administer *** for *** and ***; · Review lifestyle modifications with subject; · Review assigned titration kit to assess medication use and treatment compliance. Re-dispense kit and provide proper instructions for continued use; · Assess adverse events (including eye pain), and changes in concomitant medications; · Schedule next follow-up visit in 2 weeks (±2 days). VISIT 4: Titration: Week 4: · Collect blood sample for laboratory tests (all subjects) and perform urine pregnancy test (female subjects of childbearing potential only); · Assess weight, waist circumference, and xxxxx xxxxx; · Administer *** and ***; · Administer *** for *** and ***, and perform *** (see Section 7.4); · Review lifestyle modifications with subject; · Collect titration kit, assess treatment compliance, and perform drug accountability; · Obtain treatment kit assignment through IVRS, dispense kit to subject, and provide proper instructions for use; · Assess adverse events (includi...
Sample 1
Schedule of Visits. ‌ 9.1.1 Screening Visit (Visit 1, Up to – 4 Weeks)‌ Activities at the Screening visit are: • Obtain written parental informed consent and subject assent; • Obtain written parental informed consent and subject assent for DXA (at selected sites); • Obtain demographics (including age, gender, race, and ethnicity); • Obtain medical history (including contraception methods); • Assess inclusion/exclusion criteria; • Record concomitant medications; • Administer PHQ-9 and C-SSRS questionnaires; • Administer neurocognitive battery (CANTAB) familiarization session; • Obtain xxxxx xxxxx (blood pressure, heart rate, respiration rate, and temperature); • Obtain weight and waist circumference measurements; • Measure height and calculate BMI. If a subject does not meet the BMI criterion for inclusion into the study, no further screening procedures should be undertaken; • Obtain serum samples for blood chemistry panel, hematology panel, lipid panel, HbA1c, HIV, HCV, HBsAg, TSH; • Obtain urine sample for routine urinalysis, drug screen, and pregnancy test (female subjects); • Provide contraception/pregnancy counseling (female subjects); and • Schedule the Randomization visit within 4 weeks (± 3 days).
Sample 1

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