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OpenTrials
Completed

NCT Number: NCT00699595

Hormonal Effects on Pain Perception

To investigate if labor pain is affected by mother's hormone levels.

The hormonal effects of pregnancy are well documented. Although differences in pain sensitivity between women and men are partly attributable to social conditioning and to psychosocial factors, many laboratory studies of humans have described sex differences in sensitivity to noxious stimuli, suggesting that biological mechanisms underlie such differences. Some animal studies have suggested that sensitivity to pain decreases during pregnancy because of the progressive activation of endogenous pain inhibitory systems. This effect may be mediated by pregnancy-associated hormones, in particular progesterone.

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Key information

Age range

19 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35294, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • healthy pregnant women at term (>37GA)

Exclusion criteria

  • chronic pain
  • regular analgesic medication
  • severe cardiopulmonary problems
  • very difficult intravenous access
  • advanced labor
  • precipitous delivery

Treatment and study plan

Primary outcomes

  1. Change in heat pain threshold and tolerance

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Acronym: HEPP

Important dates

Study start
2008
Primary completion
2014
Study completion
2014
First posted
Jun 18, 2008
Registry last updated
Nov 11, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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