Literature DB >> 4159184

Sequential therapy to achieve anovulatory cycles.

G Oclander.   

Abstract

Sequential oral contraceptive therapy was devised to inhibit ovulation by a potent estrogen alone. A progestational agent was added at the end of the course of therapy to prepare the endometrium for adequate withdrawal bleeding. The program consisted of giving 80 mug. of metranol daily for 15 days and then a combination of 80 mug. of mestranol and 2 mg. of chlormadinone acetate for five additional days. Such a regimen proved to be effective in 6070 patients carefully observed for 82,085 cycles of therapy at 25 medical centres.INCREASED CYCLE REGULARITY WAS NOTED: 98.1% of the cycles were 25 to 31 days long. In 80.1% of cycles, the withdrawal interval was two to five days in length. Duration of flow was four to six days in 85.3% of the therapeutic cycles. The amount of flow decreased as compared with pretreatment values. The incidence and severity of dysmenorrhea during sequential therapy were significantly lower than before treatment. Side effects, usually infrequent, diminished as therapy was continued; the average incidence of breakthrough bleeding was 1.9% and nausea was 2.9%. Extensive laboratory studies showed no consistent abnormalities. For oral contraception, sequential therapy has proved to be virtually 100% effective when taken as directed.

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Year:  1966        PMID: 4159184      PMCID: PMC1935260     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  13 in total

1.  NEW ORAL CONTRACEPTIVE: SEQUENTIAL ESTROGEN AND PROGESTIN.

Authors:  J W GOLDZIEHER; C BECERRA; C GUAL; N B LIVINGSTON; M MAQUEO; L E MOSES; C TIETZE
Journal:  Am J Obstet Gynecol       Date:  1964-10-01       Impact factor: 8.661

2.  The effect of norethisterone and its acetate on ovarian and pituitary function during the menstrual cycle.

Authors:  J B BROWN; K FOTHERBY; J A LORAINE
Journal:  J Endocrinol       Date:  1962-12       Impact factor: 4.286

3.  CHLORMADINONE ACETATE, A NEW HIGHLY ACTIVE GESTATION-SUPPORTING AGENT.

Authors:  D M BRENNAN; R J KRAAY
Journal:  Acta Endocrinol (Copenh)       Date:  1963-11

4.  Clinical evaluation of a new oral progestin--chlormadinone.

Authors:  H DOMINGUEZ; F SIMOWITZ; R B GREENBLATT
Journal:  Am J Obstet Gynecol       Date:  1962-12-01       Impact factor: 8.661

5.  Inherent estrogenicity of norethindrone and norethynodrel: comparison with other synthetic progestins and progesterone.

Authors:  C A PAULSEN; R B LEACH; J LANMAN; N GOLDSTON; W O MADDOCK; C G HELLER
Journal:  J Clin Endocrinol Metab       Date:  1962-10       Impact factor: 5.958

6.  Comparison of the endometrial activity of 3 svnthetic progestins used in fertility control.

Authors:  M MAQUEO; E PEREZ-VEGA; J W GOLDZIEHER; J MARTINEZ-MANAUTOU; H RUDEL
Journal:  Am J Obstet Gynecol       Date:  1963-02-15       Impact factor: 8.661

7.  The influence of steroids on urinary gonadotropin excretion in a postmenopausal woman.

Authors:  E ROSEMBERG; I ENGEL
Journal:  J Clin Endocrinol Metab       Date:  1960-12       Impact factor: 5.958

8.  Progestational activity of two new compounds.

Authors:  B RUBIO
Journal:  Int J Fertil       Date:  1961 Oct-Dec

9.  Urinary OEstrogen Metabolites of 19-Norethisterone and its Esters [Summary].

Authors:  J B Brown; H A Blair
Journal:  Proc R Soc Med       Date:  1960-06

10.  Aromatization in vivo of 3 beta, 17 beta-bisacetoxy-17 alpha-ethynyl-19-norandrost-4-ene (SC-II 800).

Authors:  P K BESCH; D J WATSON; N VORYS; R D BARRY
Journal:  Biochim Biophys Acta       Date:  1963-02-05
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  1 in total

1.  Clinical evaluation of a new sequential oral contraceptive agent.

Authors:  L E Cowan
Journal:  Can Med Assoc J       Date:  1967-04-29       Impact factor: 8.262

  1 in total

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