跳至主要内容
临床试验/NCT00385892
NCT00385892终止不适用

Feasibility Study DK150OS. Testing of Compression Textile. A Safety Study Among Healthy Volonteers

Coloplast A/S0 个研究点目标入组 11 人开始时间: 2005年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Coloplast A/S
入组人数
11
主要终点
Intra Abdominal Pressure (IAP)

研究概览

简要总结

This safety study was carried out to investigate to what extent the use of an abdominal binder influences IAP. The study was designed as a comparative cross-over study measuring bladder pressure.

详细描述

Study Description: Transabdominal surgery might be associated with incisional pain, fear of rupture, inhibited mobilisation and risk of incisional herniation. An abdominal binder was developed for postoperative support of abdominal incisions. The abdominal binder provides a pressure of 10-15 mmHg.

Worlds Society on Abdominal Compartment Syndrome (WSACS) defines that Normal Intra-Abdominal Pressure (IAP) is approximately 5-7 mmHg in critically ill adults, and that Intra-Abdominal Hypertension (IAH) is a sustained or repeated pathologic elevation of IAP >12 mmHg. This safety study was carried out to investigate to what extent the use of the abdominal binder influences IAP. The study was designed as a comparative cross-over study measuring bladder pressure (Foley manometer, Holtec Medical, Copenhagen) in 11 healthy volunteers with and without wearing the abdominal binder.

Results IAP measurements without wearing the abdominal binder were found to be surprisingly high with a range between 8,0 and 16,7 mmHg. (mean 10,5 mmHg.). This finding is explained by the fact that the subjects were not under relaxation and the fact that half of the subjects according to their BMI were categorised as being overweight or fat. Other investigations have demonstrated that relaxation decreases IAP and that BMI is positively related to IAP.

We found that wearing the abdominal binder did increase IAP with a mean of 4,0 mmHg. (+/-1,4) or 39,3% (+/-14,61%).

In conclusion Relating our results to the WSACS guidelines regarding IAP and IAH it is not likely that the use of the abdominal binder will increase IAP to a clinically critical extent in patients with normal IAP. It must though be assessed from case to case, whether the use of the abdominal binder is appropriate.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Minimum 18 years old
  • •Negative test of blood, nitrate or leucocytes in urinre
  • •Waist line measurement 97-110 cm

排除标准

  • •Known allergy
  • •Know bladder disease
  • •Tendency of/clinicla symptoms of urinay infection
  • •Abdominal or urinary surgery
  • •Medical treatment

结局指标

主要结局

Intra Abdominal Pressure (IAP)

Mean Arterial Pressure (MAP)

Abdominal Perfussion Pressure (APP)

次要结局

  • Comfort
  • Freedom of movement

研究者

发起方
Coloplast A/S
申办方类型
Industry

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