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N/A N=1,533

The Possible Correlations Between the Genes Related to Pain Sensation and the Pain Sensitivity in the General Population

Pain · Surgery

Enrolled (actual)
1,533
Serious AEs
0.0%
Results posted
Feb 2015
Primary outcome: Primary: Preoperative Pressure Pain Threshold (PPT) — 2.33; 3.24 kg/cm2

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Xianwei Zhang
Primary completion
Aug 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Preoperative Pressure Pain Threshold (PPT)
2.33; 3.24
SECONDARY
Preoperative Pressure Pain Tolerance (PTO)
4.65; 6.38

Summary

Objective: This study was conducted to explore the possible correlation between some gene related to pain sensation and individual basal pain perception and postoperative pain intensity in the general population. Methods: Patients receiving elective surgery under general anesthesia were recruited into this study. The investigators measured their preoperative pressure pain threshold (PPT) and pressure pain tolerance (PTO). Pain intensity at rest and movement after the operation was evaluated . And the PCA drug consumption were recorded. Also there were healthy college students volunteer be recruited into this study. The investigators measured their experimental pain sensitivity including pressure pain threshold (PPT) and pressure pain tolerance (PTO), etc. Then genotyping was carried out.

Eligibility Criteria

Inclusion Criteria

  • •Aged 18-65 years
  • Receiving elective gynecological laparoscopic surgery
  • Anesthesiologists (ASA) physical status I or II
  • Agreed to participate the research

Exclusion Criteria

  • •History of chronic pain
  • Psychiatric diseases
  • Diabetes mellitus
  • Severe cardiovascular diseases
  • Kidney or liver diseases
  • Alcohol or drug abuse
  • Heavy smoker
  • Pregnancy or at lactation period
  • Disagree to participate to the research
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01950078). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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