ChiCTR2100042645 版本V1.1 版本创建时间2021/05/06 17:44:24 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2100042645 

最近更新日期:

Date of Last Refreshed on:

2021-05-06 17:43:05 

注册时间:

Date of Registration:

2021-01-24 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

Dr. Muhammad Usman Javed: please fill in the date of approved by ethic committee. COMPARISON OF POST-OPERATIVE ANALGESIA WITH PERI TRACT LOCAL ANESTHESIA INFILTRATION AND ORAL ANALGESIA VERSUS POST-OPERATIVE INTRAVENOUS ANALGESIA AFTER PERCUTANEOUS NEPHROLITHOTOMY. A RANDOMIZED CO

Public title:

COMPARISON OF POST-OPERATIVE ANALGESIA WITH PERI TRACT LOCAL ANESTHESIA INFILTRATION AND ORAL ANALGESIA VERSUS POST-OPERATIVE INTRAVENOUS ANALGESIA AFTER PERCUTANEOUS NEPHROLITHOTOMY. A RANDOMIZED CONTROLLED TRIAL.

注册题目简写:

English Acronym:

研究课题的正式科学名称:

COMPARISON OF POST-OPERATIVE ANALGESIA WITH PERI TRACT LOCAL ANESTHESIA INFILTRATION AND ORAL ANALGESIA VERSUS POST-OPERATIVE INTRAVENOUS ANALGESIA AFTER PERCUTANEOUS NEPHROLITHOTOMY. A RANDOMIZED CONTROLLED TRIAL.

Scientific title:

COMPARISON OF POST-OPERATIVE ANALGESIA WITH PERI TRACT LOCAL ANESTHESIA INFILTRATION AND ORAL ANALGESIA VERSUS POST-OPERATIVE INTRAVENOUS ANALGESIA AFTER PERCUTANEOUS NEPHROLITHOTOMY. A RANDOMIZED CONTROLLED TRIAL.

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

申请注册联系人:

Muhammad Usman Javed 

研究负责人:

Muhammad Usman Javed 

Applicant:

Muhammad Usman Javed 

Study leader:

Muhammad Usman Javed 

申请注册联系人电话:

Applicant telephone:

+92 33 47013969

研究负责人电话:

Study leader's
telephone:

+92 33 47013969

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

usmanjaved30@gmail.com

研究负责人电子邮件:

Study leader's E-mail:

usmanjaved30@gmail.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

498-B SAMNABAD COLONY NEAR OLD DEAF AND DUMB SCHOOL MASOOM SHAH ROAD, BAHAR CHOWK MULTAN PUNJAB PAKISTAN

研究负责人通讯地址:

498-B SAMNABAD COLONY NEAR OLD DEAF AND DUMB SCHOOL MASOOM SHAH ROAD, BAHAR CHOWK MULTAN PUNJAB PAKISTAN

Applicant address:

498-B SAMNABAD COLONY NEAR OLD DEAF AND DUMB SCHOOL MASOOM SHAH ROAD, BAHAR CHOWK MULTAN PUNJAB PAKISTAN

Study leader's address:

498-B SAMNABAD COLONY NEAR OLD DEAF AND DUMB SCHOOL MASOOM SHAH ROAD, BAHAR CHOWK MULTAN PUNJAB PAKISTAN

申请注册联系人邮政编码:

Applicant postcode:

60000

研究负责人邮政编码:

Study leader's postcode:

60000

申请人所在单位:

巴基斯坦旁遮普省拉瓦尔品第AFIU

Applicant's institution:

AFIU PUNJAB PAKISTAN

研究负责人所在单位:

巴基斯坦旁遮普省拉瓦尔品第AFIU

Affiliation of the Leader:

AFIU PUNJAB PAKISTAN

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

CPSP/REU/URO2016-118-750

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

Armed Forces Institute of Urology, AFIU, Rawalpindi

Name of the ethic committee:

Armed Forces Institute of Urology, AFIU, Rawalpindi

伦理委员会批准日期:

Date of approved by ethic committee:

1990-01-01 00:00:00

伦理委员会联系人:

Prof Muhammad Akmal

Contact Name of the ethic committee:

Prof Muhammad Akmal

伦理委员会联系地址:

AFIU, CMH Road Rawalpindi Pakistan

Contact Address of the ethic committee:

AFIU, CMH Road Rawalpindi Pakistan

伦理委员会联系人电话:

Contact phone of the ethic committee:

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

None

Primary sponsor:

None

研究实施负责(组长)单位地址:

None

Primary sponsor's address:

None

试验主办单位(项目批准或申办者):

Secondary sponsor:

经费或物资来源:

None

Source(s) of funding:

None

研究疾病:

肾石症  

Target disease:

Renal Stones

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

To compare peri tract infiltration of Bupivacaine augmented by oral post-operative analgesia versus post-operative intravenous analgesia alone in patients undergoing percutaneous nephrolithotomy in terms of mean post-operative pain score  

Objectives of Study:

To compare peri tract infiltration of Bupivacaine augmented by oral post-operative analgesia versus post-operative intravenous analgesia alone in patients undergoing percutaneous nephrolithotomy in terms of mean post-operative pain score

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

a. All patients undergoing PCNL;
b. Age from 12-65 years;
c. Normal Renal Functions;
d. No history of chronic pain;
e. ASA I, II & III;
f. Both genders.

Inclusion criteria

a. All patients undergoing PCNL;
b. Age from 12-65 years;
c. Normal Renal Functions;
d. No history of chronic pain;
e. ASA I, II & III;
f. Both genders.

排除标准:

a. History of local anesthesia allergy;
b. Redo PCNL;
c. Multiple punctures during PCNL;
d. Excessive intra-operative bleeding;
e. Diabetes Mellitus;
f. Coagulopathy;
g. Mental Disorder;
h. ASA IV & V;
i. Active urinary tract infection.

Exclusion criteria:

a. History of local anesthesia allergy;
b. Redo PCNL;
c. Multiple punctures during PCNL;
d. Excessive intra-operative bleeding;
e. Diabetes Mellitus;
f. Coagulopathy;
g. Mental Disorder;
h. ASA IV & V;
i. Active urinary tract infection.

研究实施时间:

Study execute time:

From 2019-04-11 00:00:00 To 2019-10-10 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-04-11 00:00:00 To 2019-10-10 00:00:00

干预措施:

Interventions:

组别:

A

样本量:

34

Group:

A

Sample size:

干预措施:

Local Anesthesia peri-tract of PCNL in Group A

干预措施代码:

Intervention:

Local Anesthesia peri-tract of PCNL in Group A

Intervention code:

组别:

B

样本量:

34

Group:

B

Sample size:

干预措施:

Post Op Pain after PCNL

干预措施代码:

Intervention:

Post Op Pain after PCNL

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

巴基斯坦

省(直辖市):

旁遮普 

市(区县):

拉瓦尔品第 

Country:

Pakistan

Province:

Punjab

City:

Rawalpindi

单位(医院):

AFIU 

单位级别:

三级 

Institution
hospital:

AFIU

Level of the institution:

Tertiary

测量指标:

Outcomes:

指标中文名:

Satisfactory

指标类型:

主要指标

Outcome:

Satisfactory

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Post Op Pain Score-VAS

指标类型:

次要指标

Outcome:

Post Op Pain Score-VAS

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

N/A

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 12 years
最大 Max age 65 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

lottery method

Randomization Procedure (please state who generates the random number sequence and by what method):

lottery method

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

公开/Public

盲法:

No

Blinding:

No

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

否No

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

Not stated

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Not stated

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

Not stated

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Not stated

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-01-24 10:55:06