pubmed-article:6809420 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C0034656 | lld:lifeskim |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C0021900 | lld:lifeskim |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C0597198 | lld:lifeskim |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C0699733 | lld:lifeskim |
pubmed-article:6809420 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:6809420 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:6809420 | pubmed:dateCreated | 1982-10-21 | lld:pubmed |
pubmed-article:6809420 | pubmed:abstractText | The clinical performance of two levonorgestrel-releasing intrauterine devices (IUDs) with different release rates was studied and compared with a copper-releasing Nova-T device in a randomized partly double-blind multiclinical trial. Special attention was given to patterns of bleeding, hormonal side-effects, blood pressure and body weight. The clinical acceptability of the levonorgestrel IUDs was as good as that of the copper-releasing IUD. A highly significant decrease in the amount of menstrual blood loss was seen with the levonorgestrel-IUDs, the users of which experienced fewer days of bleeding than prior to insertion. Patients suffering from dysmenorrhea experienced relief from this symptom after insertion of a levonorgestrel-IUD. Some side-effects, usually referred to as hormonal, increased during the levonorgestrel-IUD use, but did not result in higher termination rates than with the Nova-T device. No changes in body weight were recorded for the levonorgestrel-IUDs and a slight decrease in both systolic and diastolic blood pressure was found after one year of use. No infections were recorded. | lld:pubmed |
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pubmed-article:6809420 | pubmed:language | eng | lld:pubmed |
pubmed-article:6809420 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6809420 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:6809420 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6809420 | pubmed:month | Apr | lld:pubmed |
pubmed-article:6809420 | pubmed:issn | 0010-7824 | lld:pubmed |
pubmed-article:6809420 | pubmed:author | pubmed-author:DiazJJ | lld:pubmed |
pubmed-article:6809420 | pubmed:author | pubmed-author:AllonenHH | lld:pubmed |
pubmed-article:6809420 | pubmed:author | pubmed-author:LuukkainenTT | lld:pubmed |
pubmed-article:6809420 | pubmed:author | pubmed-author:NilssonC GCG | lld:pubmed |
pubmed-article:6809420 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6809420 | pubmed:volume | 25 | lld:pubmed |
pubmed-article:6809420 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6809420 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6809420 | pubmed:pagination | 345-56 | lld:pubmed |
pubmed-article:6809420 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:6809420 | pubmed:year | 1982 | lld:pubmed |
pubmed-article:6809420 | pubmed:articleTitle | Clinical performance of a new levonorgestrel-releasing intrauterine device. A randomized comparison with a nova-T-copper device. | lld:pubmed |
pubmed-article:6809420 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6809420 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:6809420 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:6809420 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:6809420 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |