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Study · Randomized controlled trial · n = 100 · 1988

6 results

Does desmopressin acetate reduce blood loss after surgery in patients on cardiopulmonary bypass?

Rocha E, Llorens R, Páramo JA, Arcas R, Cuesta B, Trenor AM

Circulation1 Jun 1988Cited by 60 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study6

6 results from studies that gave the peptide. 6 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In bypass patients, total blood loss per square meter over the first 72 hr did not differ significantly: DDAVP 458 +/- 206 ml versus placebo 536 +/- 304 ml.

    In plain wordsIn bypass patients, DDAVP did not significantly change total blood loss compared with placebo.

    Outcome
    No significant changeTotal blood loss per square meter
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Measurements

    Total blood loss per square meter, mean
    458 ml
    DDAVP group, first 72 hr
    Total blood loss per square meter, SD
    206 ml
    DDAVP group, first 72 hr
    Total blood loss per square meter, mean
    536 ml
    placebo group, first 72 hr
    Total blood loss per square meter, SD
    304 ml
    placebo group, first 72 hr

    Source sentences

    Summary
    Results showed no significant differences either in total blood loss per square meter (458 +/- 206 ml in the DDAVP group vs 536 +/- 304 ml in the placebo group) or in necessity for red cell transfusions (1642 +/- 705 ml in the DDAVP group vs 1574 +/- 645 ml in the placebo group) in the first 72 hr after surgery.
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In bypass patients, red cell transfusions over the first 72 hr did not differ significantly: DDAVP 1642 +/- 705 ml versus placebo 1574 +/- 645 ml.

    In plain wordsIn bypass patients, red cell transfusions did not differ significantly between DDAVP and placebo.

    Outcome
    No significant changeRed cell transfusions
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Measurements

    Red cell transfusion volume, mean
    1642 ml
    DDAVP group, first 72 hr
    Red cell transfusion volume, SD
    705 ml
    DDAVP group, first 72 hr
    Red cell transfusion volume, mean
    1574 ml
    placebo group, first 72 hr
    Red cell transfusion volume, SD
    645 ml
    placebo group, first 72 hr

    Source sentences

    Summary
    Results showed no significant differences either in total blood loss per square meter (458 +/- 206 ml in the DDAVP group vs 536 +/- 304 ml in the placebo group) or in necessity for red cell transfusions (1642 +/- 705 ml in the DDAVP group vs 1574 +/- 645 ml in the placebo group) in the first 72 hr after surgery.
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In bypass patients, intraoperative blood loss per square meter was lower with DDAVP (131 +/- 106 ml) than placebo (193 +/- 137 ml, p less than .02).

    In plain wordsIn bypass patients, DDAVP reduced intraoperative blood loss compared with placebo.

    Outcome
    DecreaseIntraoperative blood loss per square meter
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Measurements

    Intraoperative blood loss per square meter, mean
    131 ml
    DDAVP group
    Intraoperative blood loss per square meter, SD
    106 ml
    DDAVP group
    Intraoperative blood loss per square meter, mean
    193 ml
    placebo group
    Intraoperative blood loss per square meter, SD
    137 ml
    placebo group

    Source sentences

    Summary
    Only intraoperative blood loss per square meter was significantly lower (p less than .02) in the DDAVP group (131 +/- 106 ml) as compared with the placebo group (193 +/- 137 ml).
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In bypass patients, bleeding time prolongation at 90 min was lower with DDAVP than placebo (p less than .001).

    In plain wordsIn bypass patients, DDAVP reduced bleeding time prolongation compared with placebo.

    Outcome
    DecreaseBleeding time prolongation
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Source sentences

    Summary
    The prolongation of bleeding time and the decrease of factor VIII:C and factor VIII:von Willebrand factor 90 min after treatment were significantly lower (p less than .001) in the DDAVP group as compared with the placebo group.
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.
  5. 05HumanRandomized controlled trialMechanism

    In bypass patients, the factor VIII:C decrease at 90 min was lower with DDAVP than placebo (p less than .001).

    In plain wordsIn bypass patients, DDAVP reduced the fall in factor VIII:C compared with placebo.

    Outcome
    DecreaseFactor VIII:C decrease
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Source sentences

    Summary
    The prolongation of bleeding time and the decrease of factor VIII:C and factor VIII:von Willebrand factor 90 min after treatment were significantly lower (p less than .001) in the DDAVP group as compared with the placebo group.
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.
  6. 06HumanRandomized controlled trialMechanism

    In bypass patients, the factor VIII:von Willebrand factor decrease at 90 min was lower with DDAVP than placebo (p less than .001).

    In plain wordsIn bypass patients, DDAVP reduced the fall in factor VIII:von Willebrand factor compared with placebo.

    Outcome
    DecreaseFactor VIII:von Willebrand factor decrease
    Study

    n = 100

    Comparator
    Placebo
    Outcome group
    Bleeding and clotting · Whole body
    Studied dose
    0.3 micrograms/kgAs given in this study (human).

    Source sentences

    Summary
    The prolongation of bleeding time and the decrease of factor VIII:C and factor VIII:von Willebrand factor 90 min after treatment were significantly lower (p less than .001) in the DDAVP group as compared with the placebo group.
    2 context sentences
    Summary · context
    We have investigated the effect of DDAVP administration in a double-blind, randomized, prospective trial including 100 patients placed on cardiopulmonary bypass during surgery.
    Summary · context
    Fifty patients received 0.3 micrograms/kg DDAVP and 50 patients received a placebo administered in a 50 ml saline solution over 15 min when cardiopulmonary bypass had been concluded.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:35 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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